Food and Drug Administration - Important Food & Drug Safety Recalls

Are you on to the latest recalls? Did you know that there are health food products sold in a major health food chain stores? Organic products? Dietarty supplements that may cause liver failure and one that should only be administered by a doctor? Baby Food? and even Pet foods? Your health and wellness depends on you. Be an informed consumer :-)

As of November 13, 2013 the 3 Fellers LLC is voluntarily initiating a product recall of 3 Fellers Chocolate Cream Pies with the UPC# 891796002732 as a precautionary measure. The recall was initiated after it was discovered by the company that the product may contain undeclared almonds. People who are allergic to almonds could have a serious or life-threatening reaction if they consume this product. For consumers who are not allergic to almonds, there is no safety issue with the product. The company has received no reports of illnesses associated with this product.

This recall affects products with BEST BY DATES prior to 5/7/2014 on the bottom of the container. Products that have BEST BY DATES prior to 5/7/2014, but declare the allergen (almonds) on the label, are not included in this recall.

These products were distributed to Southern California, Virginia, Maryland, District of Columbia, Delaware, Pennsylvania, New Jersey, Ohio, and Kentucky.

No other 3 Fellers branded products are affected by this voluntary recall. Only products sold in the geographical area listed above are potentially affected.

Consumers in possession of the recalled product that have an allergy to almonds should not consume it and should discard it. Consumers with questions may contact the company at (804) 556-0671, Monday – Friday, 9am – 5pm, EDT.

Whole Foods is one of the most famous health food product stores which is a favorite of many health conscious shoppers.

November 12, 2013 - Whole Foods Market’s Northern California region is recalling ready-to-eat Artichoke Wheatberry Salad and Southwest SooFoo®* Salad in response to a recall issued today by Glass Onion Catering. The salads are being recalled as a preventive measure because they have the potential to be contaminated with E. coli O157:h7, a bacteria that may cause illness.

Symptoms of E. coli O157:H7 infection may include abdominal cramps and diarrhea which is often bloody. Most infected people recover within a week; however, some may develop complications that require hospitalization. Young children and the elderly are at highest risk for a potentially life-threatening complication known as hemolytic uremic syndrome (HUS) which includes kidney failure. To date, 26 illnesses have been reported; however, none of the illnesses are linked to products specifically sold at Whole Foods Market.

Customers may have purchased the Artichoke Wheatberry Salad and Southwest SooFoo Salad from the fresh deli case, salad bar and/or in pre-packed pint or half-pint containers in the Prepared Foods department. Both products have been pulled from all venues and carry an expiration date between Nov. 9 and Nov. 13. Four PLUs are associated with these salads:

28563300000- Artichoke Wheatberry Salad
28563400000- Artichoke Wheatberry Salad
28563700000- Southwest SooFoo Salad
28563800000- Southwest SooFoo Salad
The recalled salads were sold in the following 10 of the company’s 40 Northern California stores:

Capitola, 1710 41st Ave, Capitola, CA 95010
Fremont, 3111 Mowry Ave., Fremont, CA 94538
Oakland, 230 Bay Place, Oakland, CA 94612
Lafayette, 3502 Mt. Diablo Blvd, Lafayette, CA 94549
Los Gatos, 15980 Los Gatos Blvd, Los Gatos, CA 94032
Napa, 3682 Bel Aire Plaza, Napa, CA 94558
Noe Valley, 3950 24th St, San Francisco, CA 94114
Redwood City, 1250 Jefferson Ave, Redwood City, CA 94062
San Mateo, 1010 Park Pl, San Mateo, CA 94403
Walnut Creek, 1333 Newell Ave, Walnut Creek, CA 94596
Customers who have purchased these products should discard them, and may bring in a receipt to any of the above stores for a full refund.

Questions about the recall can be directed to 512-477-5566, ext. 20060, Monday-Friday from 8 a.m. to 5 p.m. CST.


On November 11, 2013 - Palmer Candy Company of Sioux City, IA is recalling 102 cases of HyVee Chocolate Caramel Clusters and 90 cases HyVee Chocolate Covered Caramels because they may contain undeclared peanuts. People who have an allergy to peanuts run the risk of a serious or life-threatening allergic reaction if they consume these products.

The recalled product was distributed throughout the Midwest to HyVee Stores.

The recalled products can be identified by the following:

HyVee Chocolate Caramel Clusters – UPC 7723212515 9 oz plastic tub with the following lot code: Sell By: 04/07/14 F30202 located on the bottom of each tub.
HyVee Chocolate Covered Caramels – UPC 7723212520 12 oz plastic tub with the following lot code: Sell By: 10/07/14 F30202 located on the bottom of each tub.
No illnesses have been reported in connection with either of the products being recalled.

The recall was initiated after it was discovered that the HyVee Chocolate Caramel Clusters were mispackaged in HyVee Chocolate Covered Caramel labels. The HyVee Chocolate Covered Caramel label does not list peanuts as an ingredient.

Consumers who have purchased HyVee Chocolate Caramel Clusters or HyVee Chocolate Covered Caramels are urged to return it to the place of purchase for a full refund. Consumers with questions may contact Palmer Candy Company (800) 831-0828, Monday – Friday, 8:00 AM – 4:30 PM.


While trying to lose weight, some may turn to supplements to give them a boost. However on November 9, 2013 – USPlabs LLC, Dallas, TX is voluntarily conducting a national recall of all lots and sizes of the OxyElite Pro dietary supplement products listed below. These products contain Aegeline, a synthesized version of a natural extract from the Bael tree.

Epidemiological evidence shows that use of these products has been associated with serious adverse health consequences, namely serious liver damage or acute liver failure, concentrated in Hawaii. Investigations are ongoing into a potential causal relationship. The Company agrees with FDA that a national recall is appropriate as a precautionary measure. Product was distributed nationwide through retail stores, mail orders and direct delivery.

OxyElite Pro Super Thermo capsules
2 count capsules UPC #094922417275
10 count capsules UPC #094922417251
10 count capsules UPC #094922417268
21 count capsules UPC #094922426604
90 count capsules UPC #094922395573
90 count capsules "Pink label" UPC #094922447906
180 count capsules UPC #094922447852

OxyElite Pro Ultra-Intense Thermo capsules
3 count capsules UPC #094922447883
3 count capsules UPC #094922447876
90 count capsules UPC #094922395627
180 count capsules UPC #094922447869

OxyElite Pro Super Thermo Powder
Fruit Punch 0.15 oz UPC #094922417237
Fruit Punch 0.15 oz UPC #094922447517
Fruit Punch 4.6 oz UPC #094922426369
Fruit Punch 5 oz. UPC #094922447487
Blue Raspberry 4.6 oz UPC #094922426376
Grape Bubblegum 4.6 oz UPC #094922447500
Green Apple 4.6 oz. UPC #094922426499

No other products produced by USPlabs are subject to recall. Consumers who have purchased the products should immediately discontinue use of the product and return it to where they purchased it for a refund. Contact your health care professional if you have experienced any adverse effects.

Consumers can contact USPlabs at 1(800) 890-3067 (Monday-Friday, 9 am - 5 pm EST) or info@usplabsdirect.com. Adverse reactions may be reported to the FDA MedWatch Adverse Event Reporting program online at http://www.fda.gov/medwatch/getforms.htm, by regular mail, or by FDA's MedWatch Hotline 1-800-FDA-1088.


November 8, 2013 — Sequel Naturals Inc., dba “Vega,” announced today that it has taken the precautionary measure of voluntarily withdrawing a limited quantity of its Vega One Nutritional Shakes and Sports Performance Protein products due to finding trace amounts of chloramphenicol (CAP), a naturally occurring antibiotic.

Chloramphenicol is a prescription drug commonly used to treat typhoid fever and eye infections around the world. It should only be used under medical supervision. It has been associated with rare cases of aplastic anemia and allergic reactions in some people. A leading expert on CAP says that there have been no known cases of anemia caused by residual amounts found in food. Pregnant or lactating women should avoid this medication.

None of the Vega product formulations include CAP as an ingredient; however, an enzyme that was provided by a third party supplier, which constitutes less than 1% of the product ingredients, was found to contain trace amounts of CAP.

As a precautionary measure, Vega is voluntarily withdrawing all of the listed product from the market and has taken steps to ensure all future products are CAP-free, including using a different source of enzymes to prevent further potential contamination and assure consumers of product purity. These actions complete a voluntary product withdrawal and ingredient resourcing that applied to Canadian products as well.

“We’re doing this out of an overabundance of caution and to ensure that when you go to the shelf, you never have to wonder about the purity of a Vega product,” said Charles Chang, Vega President and Founder.

The Vega products were distributed nationwide in retail stores.

People who have severe sensitivity or allergies to chloramphenicol may run the risk of an allergic reaction if they consume these products. There have been no reported allergic reactions from the listed products. See complete table HERE


Oh baby, baby food on November 8, 2013 – Plum Organics is voluntarily recalling pouch products within its Baby Stage 2, Tots Mish Mash and Kids lines after discovering a manufacturing defect that may cause spoilage in some pouches. Recalled products can be identified by the “Best By” dates ranging from 08/05/14 to 12/08/14 and the letters “AT.” Consumers can find a list of affected products at www.plumorganics.com/Nov13Recall.pdf.

Plum has determined that the potential spoilage may cause some pouches to swell. Out of an abundance of caution, Plum is removing all pouches with affected codes.

Parents should not feed any of these products to their children. Consumers who have purchased affected products should contact the Plum Organics Consumer Hotline at 866-495-3774 or send an email to info@plumorganics.com to request a product replacement voucher.

“As a father of two, I know how it feels to want nothing but the very best for our kids and yours,” said Neil Grimmer, president and co-founder of Plum Organics. “Over the years, Plum has worked hard to earn the trust of parents, and we fully intend on maintaining that trust. We are taking every action to ensure that our highest standards are being met.”


And now we share another recall for an important member of the family. On November 4, 2013 - Bailey's Choice LLC. in Waleska, GA is recalling its 5 oz. packages of chicken treats because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

The Bailey's Choice Dog Treats included in this expanded recall are the following five-ounce packages of dog treats:

100% Chicken Treat, lot # "Jun 2 2013" sold in Georgia only
100% Chicken Treat, lot # "Jun 3 2013" sold in Georgia only
100% Chicken Breast Treat, lot # "Jun 4 2013" sold in Georgia only
100% Chicken Treat, lot # "Jun 15 2013" sold in Georgia only
100% Chicken Treat, lot # "Jul 8 2013" sold in Georgia only
100% Chicken Treat, lot # "Jul 11 2013" sold in Georgia only
100% Teriyaki Chicken Treat, lot # 132881 sold in Georgia and North Carolina
The potential for contamination was noted after routine testing by the Georgia Department of Agriculture (GDA) revealed the presence of Salmonella in some 5 oz. packages of chicken treats.

Production of the product has been suspended while GDA and the company continue their investigation as to the source of the problem. The FDA is monitoring the situation.

Consumers who have purchased 5 oz. packages of Bailey's Choice chicken treats are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 770-881-0526 between 9:00AM and 6:00PM EST.

For more recalls - FDA SAFETY RECALLS

What do you know about the Latest Recall?

It's so important to know what the latest recalls are just in case you happen to have them in your home. While I may be wrong, I do not think that there are many people who are checking daily to see if there is a recall on any item in their home before they eat. Can you imagine waking up with these mini butter or chocolate croissants ready and available in your kitchen? Would you check in with the FDA or the company's website to see if there is a recall? Of course not. Well, there is a recall on these items and more.
Pull up your chair and prepare to check your list. This is quite a long list as reported via FDA.

Posh Bakery of Santa Clara, CA is recalling all its Butter Mini Croissants and Chocolate Mini-Croissants due to use of an egg wash that was undeclared on the product label. People who have allergies to eggs run the risk of serious or life-threatening reactions if they consume this product.

The product was sold to the following 26 Whole Foods Market stores in Northern California:



Berkeley
Blithedale (Mill Valley)
Blossom Hill (San Jose)
Campbell
Coddingtown (Santa Rosa)
Franklin (San Francisco)
Harrison (Oakland)
Lafayette
Los Altos
Los Gatos
Mill Valley
Napa
Petaluma
Potrero Hill (San Francisco)
Redwood City
Roseville
Sacramento
San Mateo
San Rafael
San Ramon
Santa Cruz
Santa Rosa
South of Market (San Francisco)
Stanyan (San Francisco)
Stevens Creek (Cupertino)
Walnut Creek

The products came in 12-pack, 12-ounce, clear, plastic clamshell containers and were sold with Whole Foods Market labels, specifically “Croissants Mini Butter 12PC Whole Foods,” UPC: 21609300000, and “Croissant Mini Chocolate 12PC,” UPC: 21609400000. The recall includes all expiration best-buy dates and lot codes. The recall includes all expiration best-buy dates and lot codes prior to and up until July 6, 2011.

One allergic reaction has been reported. Consumers who have purchased “Croissants Mini Butter 12PC Whole Foods,” and “Croissant Mini Chocolate 12PC,” may return the product to the place of purchase for a full refund. Consumers with questions may contact at Posh Bakery at (408) 980-8451 Monday to Friday 9:00am to 5:00pm PDT.

Now this is totally important to ALL MEN WHOM IT MAY CONCERN:

Global Wellness, LLC. Hollywood, FL is expanding its voluntary nationwide recall of VIA XTREME ULTIMATE SEXUAL ENHANCER DIETARY SUPPLEMENT FOR MEN to the consumer level to include lot A032111. The product was distributed throughout the U.S. Puerto Rico, Barbados, and Canada to internet and retail consumers. The product is distributed as a bottle containing six (6) blue colored capsules per package. The label on the packaging lists the company name Global Wellness, LLC, Hollywood Florida.

Lot numbers #809013, 806030, and A032111 are covered in this recall.

The company has been informed by representatives of the Food and Drug Administration (FDA) that laboratory analysis conducted by FDA for lot #809013, 806030, and A032111 found that the product contains sulfoaildenafil methanesulfonate, sulfosildenafil and dimethylsildenafil analogs of sildenafil. Sildenafil is an active ingredient of an FDA approved drug for erectile dysfunction (ED), making Via Xtreme Ultimate Sexual Enhancer Dietary Supplement for Men an unapproved drug. The active drug ingredient is not listed on the product label. The undeclared ingredient may interact with nitrates found in some prescription drugs such as nitroglycerin and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Additionally, the product may cause side effects, such as headaches and flushing.

No illnesses have been reported to Global Wellness, LLC to date in connection with these products.

With an abundance of caution, Global Wellness, LLC is expanding its voluntary recall to include lot numbers #809013, 806030, and A032111. VIA XTREME ULTIMATE SEXUAL ENHANCER DIETARY SUPPLEMENT FOR MEN. This recall does not affect sales and distribution of SLIM XTREME GOLD™ and GELSLIM™.

Customers who have this product in their possession should stop using it immediately and contact their physician if they have experienced any problems that may be related to taking this product.

Any adverse events that may be related to the use of this product should be reported to the FDA’s MedWatch Adverse Event Reporting program online [at www.fda.gov/MedWatch/report.htm], by phone [1-800-FDA-1088], or by returning the postage-paid FDA form 3500 [which may be downloaded from www.fda.gov/MedWatch/getforms.htm] by mail [to MedWatch, 5600 Fishers Lane, Rockville, MD 20852-9787] or fax [1-800-FDA-0178].

Consumers with questions may contact the company at (954) 922-1133 Monday through Friday from 9:00am to 4:00pm EST for instructions on the return process.
Global Wellness, LLC apologizes for any inconvenience and expresses its concerns for the health of consumers by conducting a voluntary recall action.

Where's the Enchilada Sauce? HOLD IT RIGHT THERE - PLEASE CHECK THE LABEL

Arizona Canning Company is recalling its 29 ounce cans of Sun Vista Red Enchilada Sauce (Mild, Medium and Hot) because they may contain undeclared soy protein. People, who have allergies to soy, run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled Sun Vista Red Enchilada Sauce (Mild, Medium and Hot) was distributed in California and Arizona. All lots of this product are being recalled.

No illnesses have been reported to date in connection with this problem.

The recall was initiated after it was discovered that the ingredient list on the label reads “Hydrolyzed Vegetable Protein” instead of the more descriptive term “Hydrolyzed Vegetable Protein (Soy)”.

Consumers who have purchased the Sun Vista Red Enchilada Sauce (Mild, Medium and Hot) and are sensitive or allergic to Soy are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-211-0600 (Mon-Fri 7:30AM-4:00PM (MST)).

Do you have any more Uneviscerated Fish? Well, this is no laughing matter.....

Euphoria Fancy Food Inc. 149-151 2nd Ave. Brooklyn NY 11215 is recalling Herring Special Salting discovered by New York State Department of Agriculture and Markets Food Inspectors during a routine inspection and subsequent analysis of product by Food Laboratory personnel confirming that the fish was not properly eviscerated prior to processing.

This product may be contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food-borne illness.

The sale of this type of fish is prohibited under New York State Agriculture and Markets regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of botulism poisoning. Symptoms of botulism include blurred or double vision, general weakness, poor reflexes, difficulty in swallowing and respiratory paralysis.

The recalled Herring Special Salting comes in an uncoded, 48.58oz (1300gr) plastic container and is a product of Russia. Herring Special Salting was sold in New York State.

No illnesses have been reported to date in connection with this problem. Consumers who have Herring Special Salting are advised not to eat it, but should return it to the place of purchase. Consumers with questions may contact the company at 718-768-3400.

All weight loss dietary supplements consumers:

Intercharm Inc., is recalling Slimforte Slimming Capsules, Slimforte Slimming Coffee, and Botanical Slimming Soft Gel to the consumer/user level. FDA laboratory analyses found the products to contain Sibutramine an appetite suppressant. Sibutramine is a controlled substance that was withdrawn from the market in October 2010 for safety reasons.

Slim Forte Slimming Capsules is packaged in a green box with a picture of a woman on the front. The box has pink, blue, and green text. The box contains 30 capsules.
Slim Forte Slimming Coffee is packaged in a green box with a picture of a woman on the front. The box has pink, blue, and green text. The box contains 10 packets of instant coffee.
Meizitang Botanical Slimming Soft Gel is packaged in a green package/pouch with green background and a picture of a woman on front. The package has yellow, white, and black text. The pouch contains 3 blister packs of 12 each 650 mg softgel capsules.
Products containing Sibutramine pose a threat to consumers because Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. These products may also interact in life threatening ways with other medications a consumer may be taking. Intercharm Inc. has not received any reports of adverse events related to this recall.

These products are sold as dietary supplements and marketed for weight loss. Slim Forte Slimming Capsule, Batch No. 20100928, Best By 09.27.2012 and Batch No. 20100604, Best By 06.03.2012; Slim Forte Slimming Coffee, Batch No. 20100903, Best By 09.02.2012; and Meizitang Botanical Slimming Soft Gel, Lot Code 12.24.2009, Best By 12.23.2011 are included in this recall. Products were distributed through the internet nationwide and internationally to Ireland.

Consumers should stop using these products immediately and return to the place of purchase. Consumers who have experienced any negative side effects should consult a health care professional as soon as possible.

Any questions related to this recall should be directed to Intercharm Inc. at 323-876-7441 Monday through Friday 8:00 AM to 4:30 PM, EST.

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program online, by regular mail, or by fax.

Online: www.fda.gov/medwatch/report.htm
Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at: www.fda.gov/MedWatch/getforms.htm. Mail to address on the pre-addressed form.
Fax: 1-800-FDA-0178.

Did I warn you that this was going to be a long one? Well, here goes -->

Flying Food Group’s Lawrenceville, GA facility is recalling all USDA and FDA regulated products (sandwiches, parfaits, wraps, plates, and salads) because they have the potential to be contaminated with Listeria monocytogenes. No illnesses have been reported to date in connection with this problem.

Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women

This recall is an expansion of one initiated on July 19th at USDA’s request. The expanded recall includes products made for Core-mark Atlanta Division, Race Trac, and Starbucks. Core-mark Atlanta Division products were distributed to retail outlets in Alabama, Georgia and Florida. Starbucks products were only distributed to retail outlets in Alabama and Georgia. Race Trac products were distributed to retail outlets in Georgia only.

The following are the list of additional FDA and USDA regulated products implicated in this recall:

Core-mark Atlanta Division (distributed in Alabama, Georgia, Florida):

· 8.5 ounce packages of “Sano Very Berry Yogurt Parfait” that have “Enjoy By” dates of 7/23 – 8/3

· 8.0 ounce packages of “Sano Triple Cherry Yogurt Parfait” that have “Enjoy By” dates of 7/23 – 8/3

· 6.4 ounce trays of “F & L Café Salad, Chicken Caesar Salad” that have “Best Before” dates of 7/23 – 8/3*

· 6.9 ounce trays of “F&L Café Salad, Chef Salad” that have “Best Before” dates of 7/23 – 8/3*

Race Trac (distributed in Georiga):

· 9.05 ounce packages of “Turkey Quarter Pounder with Tomatoes” that have “Sell Thru” dates of 7/17 -7/28

· 4.95 ounce packages of “Egg Salad” that have “Sell Thru” dates of 7/17-7/28

· 4.95 ounce packages of “Chicken Salad” that have “Sell Thru” dates of 7/17-7/28

· 7.8 ounce packages of “Chicken Quarter Pounder” that have “Sell Thru” dates of 7/17-7/28

· 7.38 ounce packages of “Turkey Quarter Pounder” that have “Sell Thru” dates of 7/17 – 7/28

· 8.8 ounce packages of “Chicken Quarter Pounder with Tomatoes” that have “Sell Thru” dates of 7/17-7/28

· 8.4 ounce packages of “Jumbo BBQ Pork Sandwich” that have “Sell Thru” dates of 7/17-7/28

· 7.38 ounce packages of “Ham Quarter Pounder” that have “Sell Thru” dates of 7/17-7/28

· 9.05 ounce packages of “Ham Quarter Pounder with Tomatoes” that have “Sell Thru” dates of 7/17-7/28

· 10.17 ounce packages of “American Sub” that have “Sell Thru” dates of 7/17-7/28

· 5.57 ounce packages of “Tuna Salad” that have “Sell Thru” dates of 7/17-7/28

· 9.75 ounce packages of “Turkey Wrap” that have “Sell Thru” dates of 7/17 – 7/28*

· 10.3 ounce packages of “Chicken Caesar Salad” that have “Sell Thru” dates of 7/17 – 7/28*

· 7.88 ounce packages of “Chicken Caesar Wrap” that have “Sell Thru” dates of 7/17 – 7/28*

· 9.8 ounce packages of “Cobb Salad” that have “Sell Thru” dates of 7/17-7/28*

Starbucks (distributed in Georgia and Alabama):

· 6.6 ounce packages of “Egg Salad Sandwich” that have “Enjoy By” dates of 7/15-7/26

· 5.9 ounce package of “Chicken Chipotle” that have “Enjoy By” dates of 7/15-7/26

· 7.5 ounce package of “Tarragon Chicken Salad Sandwich” that have “Enjoy By” dates of 7/15-7/26

· 5.0 ounce package of “Roma Tomato & Mozzarella” that have “Enjoy By” dates of 7/15-7/26

· 6.4 ounce package of “Turkey and Swiss Sandwich” that have “Enjoy By” dates of 7/15-7/26

· 5.5 ounce package of “Ham and Swiss” that have “Enjoy By” dates of 7/15-7/26

· 8.1 ounce package of “Strawberry and Blueberry Yogurt Parfait” that have “Enjoy By” dates of 7/16-7/27

· 8.1 ounce package of “Dark Cherry Yogurt Parfait” that have “Enjoy By” dates of 7/16-7/27

· 6.1 ounce package of “Greek Yogurt & Honey Parfait” that have “Enjoy By” dates of 7/16-7/27

· 8.3 ounce package of “Sesame Noodles Bistro Box” that have “Enjoy By” dates of 7/15 – 7/26

· 5.3 ounce package of “Cheese & Fruit Bistro Box” that have “Enjoy By” dates of 7/15-7/26

· 6.8 ounce package of “Protein Bistro Box” that have “Enjoy By” dates of 7/15-7/26

· 5.9 ounce package of “Tuna Salad Plate Bistro Box” that have “Enjoy By” dates of 7/15-7/26

· 5.1 ounce package of “Hot Panini Roasted Tomato & Mozzarella” that have “Enjoy By” dates of 7/15-7/26

· 6.1 ounce package of “Hot Panini Roasted Vegetable” that have “Enjoy By” dates of 7/15-7/26

· 6.1 ounce package of “Hot Panini Chicken Santa Fe” that have “Enjoy By” dates of 7/15-7/26

· 5.2 ounce package of “Hot Panini Ham & Swiss” that have “Enjoy By’ dates of 7/15-7/26

· 8.4 ounce package of “Chipotle Chicken Wraps Bistro Box” that have “Enjoy By” dates of 7/16-7/26*

· 6.3 ounce package of “Chicken & Hummus Bistro Box” that have “Enjoy By” dates of 7/16-7/26*

· 4.6 ounce package of “Salumi & Cheese Bistro Box” that have “Enjoy By” dates of 7/15-7/26*

· 7.3 ounce package of “Chicken Lettuce Wraps Bistro Box” that have “Enjoy By” dates of 7/15-7/26*

*These packages bear the USDA establishment number "P-34373" or EST. 34373 inside the USDA mark of inspection.

Again, no illnesses have been reported to date in connection with this problem.

The potential for contamination was noted after sampling and testing conducted by the Georgia Department of Agriculture revealed the presence of Listeria monocytogenes in one of the products.

The production of all products at the Lawrenceville, GA facility has been voluntarily suspended pending a full investigation into the source of the problem.

Consumers who determine they have affected product should destroy that product or return it to the location where purchased for a full refund.

Consumers with questions may contact the company‘s representative, Ellen Pritsker at (312) 243-2122 ext. 127 during the hours of 9 AM to 5 PM Monday through Friday. Voice mail messages may also be left and will be returned. Emails may also be sent to epritsker@flyingfood.com.

Now your pet needs are also essential as veterinarian fees can be costly?

Nestlé Purina PetCare Company (NPPC) is voluntarily recalling a limited number of 3.5- and 7-pound bags of its Purina ONE Vibrant Maturity 7+ Dry Cat Food from a single production run and shipped to customers in 12 states in December 2010. This is being done because some bags of the product have been found to be contaminated with Salmonella. Only Purina ONE Vibrant Maturity 7+ Dry Cat Food with both the “Best By” date and the production code shown are included in this voluntary recall :


Product Name Bag size “Best By”Date & Production Code* Bag UPC Code
Purina ONE Vibrant Maturity 7+ 3.5lb. MAY 2012 03341084 17800 01885
Purina ONE Vibrant Maturity 7+ 3.5 lb. MAY 2012 03351084 17800 01885
Purina ONE Vibrant Maturity 7+ 7 lb. MAY 2012 03341084 17800 01887
Purina ONE Vibrant Maturity 7+ 7 lb. MAY 2012 03351084 17800 01887


*”Best By” Date and Production Code are found on the back or bottom of the bag.

No additional Purina cat or dog products are involved in this voluntary recall. No other Purina ONE brand products are involved. Only Purina ONE Vibrant Maturity 7+ brand products which match the “Best By” dates and production code above are included in this recall.

Consumers who have purchased Purina ONE Vibrant Maturity 7+ Dry Cat Food products with these specific “Best By” Date and Production Codes should discontinue feeding the product and discard it.

Salmonella can affect animals eating the product, and there is a risk to humans from handling contaminated products. People handling contaminated dry pet food can become infected with Salmonella, especially if they have not thoroughly washed their hands after having contact with surfaces exposed to this product. Healthy people infected with Salmonella should monitor themselves for the following symptoms: nausea, vomiting, diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments including arterial infections, endocarditis, arthritis, muscle pain, eye irritation and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.

Pets with Salmonella infections may exhibit decreased appetite, fever and abdominal pain. If left untreated, pets may be lethargic and have diarrhea or bloody diarrhea, fever and vomiting. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If you pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

The product was distributed to customers located in California, Iowa, Illinois, Indiana, Kentucky, Michigan, Minnesota, Missouri, North Dakota, Nebraska, Ohio and Wisconsin, who may have further distributed the product to other states.

Nestlé Purina PetCare Company became aware of the contamination as a result of samples that had been collected in several retail stores.

At Nestlé Purina PetCare, the safety and efficacy of our products are our top priority. We apologize for any inconvenience due to this voluntary recall. For further information or to obtain a product refund, please call NPPC toll-free at 1-800-982-6559 or visit www.purina.com.

H-E-B is encouraging customers to check their refrigerators for 8 oz, 16 oz, 24 oz and 32 oz sizes of H-E-B Brand cottage cheese, dips, yogurt and sour cream sold between June 18 and July 27. The products, sold at H-E-B, Central Market, Mi Tienda and Joe V’s, are being recalled as a precaution due to the possible presence of foreign material. 4 oz and 6 oz sizes are not impacted by the recall.

While no reports of injury have been received, the voluntary recall has been issued by H-E-B, in an abundance of caution, to ensure the safety of its customers.

“H-E-B is committed to the highest standards of food safety for our customers,” said Winell Herron, Group Vice President of Public Affairs and Diversity. “We want to take every precaution necessary to ensure the integrity and quality of the products sold in our stores.”

Customers can return the recalled products to any H-E-B, Central Market, Mi Tienda and Joe V’s store for a full refund. Customers with concerns or questions may contact H-E-B Customer Relations at 210-938-8357 or 1-800-432-3113

Below is the list of products affected by the recall:


Product Name UPC Code Size
H-E-B Cottage Cheese w/Pineapple 0004122024784 16 Oz
H-E-B Small Curd Cottage Cheese 0004122095829 16 Oz
H-E-B Small Curd Cottage Cheese 0004122086701 24 Oz
H-E-B Fat Free Cottage Cheese 0004122024778 16 Oz
H-E-B Low Fat Cottage Cheese 0004122024782 16 Oz
H-E-B Low Fat Cottage Cheese 0004122055145 24 Oz
H-E-B Large Curd Cottage Cheese 0004122083891 16 Oz
H-E-B Large Curd Cottage Cheese 0004122068689 24 Oz
H-E-B Fat Free Cottage Cheese 0004122066631 24 Oz
H-E-B French Onion Party Dip 0004122074261 8 Oz
H-E-B Jalapeno Dip 0004122083489 8 Oz
-E-B Green/Onion Party Dip 0004122055596 8 Oz
H-E-B Ranch Style Dip 0004122077256 8 Oz
H-E-B Chili Con Queso Dip 0004122039858 8 Oz
H-E-B French Onion Party Dip 0004122045014 16 Oz
H-E-B Ranch Style Dip 0004122052078 16 Oz
H-E-B Chili Con Queso Dip 0004122052077 16 Oz
H-E-B Roasted Garlic Dip 0004122080646 8 Oz
H-E-B French Onion Dip 0004122024522 24 Oz
H-E-B Sour Cream 0004122026665 8 Oz
H-E-B Sour Cream 0004122025475 16 Oz
H-E-B Sour Cream 0004122052076 24 Oz
H-E-B Light Sour Cream 0004122066383 24 Oz
H-E-B Light Sour Cream 0004122072487 16 Oz
H-E-B Light Sour Cream 0004122010555 8 Oz
H-E-B Fat Free Sour Cream 0004122000517 16 Oz
H-E-B Sweetened Plain Yogurt 0004122030330 32 Oz
H-E-B Blended Vanilla Yogurt 0004122030329 32 Oz
H-E-B Blended Peach Yogurt 0004122030328 32 Oz
H-E-B Blended Strawberry Yogurt 0004122030327 32 Oz
H-E-B Light Strawberry Yogurt 0004122030325 32 Oz
H-E-B Light Vanilla Yogurt 0004122030326 32 Oz
H-E-B Fat Free Active Tub Vanilla 0004122030196 24 Oz
H-E-B Fat Free Active Tub Plain 0004122030195 24 Oz
H-E-B Low Fat Active Tub Strawberry 0004122030194 24 Oz
H-E-B Low Fat Active Tub Vanilla 0004122030193 24 Oz

Dole Fresh Vegetables is voluntarily recalling 2,880 cases of DOLE® Italian Blend salad with Use-by Date of June 19, 2011, UPC code 7143000819 and Product Codes 0049A157201A, 0049A157201B, 0049A157202A, 0049A157202B, 0686A157202A, 0686A157202B and 442 cases of Kroger Fresh Selections Italian Style Blend salad with Use-by-Date of June 19, 2011, UPC code 1111091045 and Product Codes A157201A & A157201B, due to a possible health risk from Listeria monocytogenes. Dole Fresh Vegetables is coordinating closely with regulatory officials. No illnesses have been reported in association with the recall.

The Product Code and Use-by Date are in the upper right-hand corner of the package; the UPC code is on the back of the package, below the barcode. The salads were distributed in twelve U.S. states (Illinois, Indiana, Kentucky, Maine, Michigan, Mississippi, New Jersey, New York, Ohio, Pennsylvania, Tennessee and Wisconsin) and three Canadian provinces (New Brunswick, Ontario and Quebec).

No illnesses have been reported in association with the recall. This precautionary recall notification is being issued due to an isolated instance in which one package of Dole Italian Blend salad yielded a positive result for Listeria monocytogenes in a random sample test collected and conducted by the Ohio Department of Agriculture.

No other Dole or Kroger salads are included in the recall. Only the specific Product Codes, UPC codes and June 19, 2011 Use-by-Date of Italian Blend salads identified above are included in the recall. Consumers who have any remaining product with these Product Codes should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Food Company Consumer Response Center at (800) 356-3111, which is open 8:00 am to 3:00 pm (PDT) Monday - Friday.

Retailers should check their inventories and store shelves to confirm that none of the product is mistakenly present or available for purchase by consumers or in warehouse inventories. Dole Fresh Vegetables customer service representatives are already contacting retailers and are in the process of confirming that the recalled product is not in the stream of commerce.

Listeria monocytogenes is a bacterium that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastrointestinal symptoms such as nausea or diarrhea. If it spreads to the nervous system symptoms may include headache, stiff neck or confusion. The illness primarily impacts pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.

One of my favorites is being recalled again :-(

McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling at the retail level one product lot (60,912 bottles) of TYLENOL®, Extra Strength Caplets, 225 count bottles, distributed in the U.S. The recalled product was manufactured in February, 2009. McNeil is taking this action following a small number of odor reports, including musty, moldy odor. The uncharacteristic musty, moldy odor has been linked to the presence of trace amounts of a chemical known as 2,4,6-tribromoanisole (TBA).

This voluntary action is being taken as a precaution and the risk of serious adverse medical events is remote. TBA can generate an offensive odor and has been associated with temporary and non-serious gastrointestinal symptoms.

The product lot number for the recalled product can be found on the side of the bottle label.

FULL RECALLED PRODUCT LIST:

Product Name Lot Number UPC Code
TYLENOL®, Extra Strength Caplets, 225 count ABA619 300450444271

Consumers who purchased product from the lot included in this recall should stop using the product and contact McNeil Consumer Healthcare, either at www.tylenol.com or by calling 1-888-222-6036 (Monday-Friday 8 a.m. to 8 p.m. Eastern Time) for instructions about receiving a refund or product coupon. Consumers who have medical concerns or questions should contact their healthcare provider.

Any adverse reactions may also be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Online:www.fda.gov/medwatch/report.htm
Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at: www.fda.gov/MedWatch/getforms.htm. Mail to address on the pre-addressed form.
Fax: 1-800-FDA-0178

Seafood Lovers....... pay attention!

Risvold’s Salads Inc of Gardena, CA is recalling seafood salad and seafood pasta salad, because it may contain undeclared milk, sunflower, sesame and soy. People who have an allergy or severe sensitivity to milk, sunflower, sesame and soy run the risk of serious or life-threatening allergic reaction if they consume these products.


Item Number of Cases Use By Date
Seafood Pasta 3 7/17/11
Seafood Salad 24 6/27/11
Seafood Salad 29 7/4/11
Seafood Salad 60 7/11/11
Seafood salad and seafood pasta were distributed in Nevada, Oregon, Washington, Montana and Idaho. All products were sold behind the deli case in select retail markets. The code dates for the seafood salad in question are all dates prior to “use by” of 071111 and for the seafood pasta all dates prior to “use by” of 071711. All products has been pulled from store/vendor shelves and destroyed as of June 22, 2011.

No illnesses have been reported to date.

The recall was initiated during a routine FDA yearly audit, it was discovered that product containing milk, sunflower, sesame and soy was distributed in packaging that did not reveal the presence of milk, sunflower, sesame and soy. Subsequent investigation indicates the problem was caused by a change of ingredient being supplied by a vendor.

The problem was corrected immediately and all items PAST the above mention “use by” dates are safe for consumption and correct labeling has been applied.

Consumers who have purchased Risvold’s seafood salad and seafood pasta are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at (323) 770-2674, Mon-Fri 7:30am–4pm(PST).

Warts and all........

Nature Relief is voluntarily recalling Nature Relief Instant Wart and Mole Remover. Consumers are advised to discontinue use and immediately dispose of any used or unused portions of the product. It is suggested that you discard of the product and contents inside a plastic bag and place it into the garbage for safe and quick disposal, in order to expedite the recall process and avoid further handling.

The recall is effective immediately and is being undertaken voluntarily in conjunction with the FDA because the product is potentially unsafe and contains an ingredient that may result in harmful burns to the skin that was previously unknown by the company.

The FDA has advised that the active ingredient, calcium oxide, can cause severe burns of the skin, particularly to areas of thin or sensitive skin, such as the face, area around the eyes, and genitalia. The FDA has received a report of an injury associated with the use of this product, including burns to the skin that required medical attention.

In addition, the FDA advises that consumers are recommended to have moles reviewed by licensed medical professionals and ensure they are not cancerous. Moles when left untreated can possibly lead to melanoma a form of cancer and self-treatment of diseases such as cancer can cause a delay in early diagnosis, which may help prevent life threatening complications.

This product is sold as a kit, which contains the following items: two small containers labeled "Repair Cream", one container of "Antiseptic Wash", a package of "Triple Antibiotic Ointment", toothpicks, and a "vanity kit" with cotton balls, swabs, and nail files.

This recall is being made in cooperation with the US Food and Drug Administration.

Consumers who purchased NatureRelief Instant Wart and Mole Remover should immediately discontinue their use and discard the remaining contents. Consumers with questions may contact Nature Relief customer care at 1-888-646-6399 or email the company at support@naturerelief.com.

Consumers who experience adverse events with this product should seek immediate help from their physician or healthcare provider.

Nature Relief is a 5-month-old small start up company that operated with 1 employee and only sold a very small quantity of the product through direct to consumer Internet marketing. No sales were conducting with distributors, wholesalers or retailers. Nature Relief did not turn a profit and revenue was only generated through the sales of the one product "Instant Wart Mole Remover".

All sales and operations of Nature Relief have now been temporally ceased.

Any adverse reactions experienced with the use of this product should also be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088, by fax at 1-800-FDA-0178, by mail at Med Watch, HF-410, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the Med Watch website at www.fda.gov/medwatch.