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.
The product was sold to the following 26 Whole Foods Market stores in Northern California:
Blithedale (Mill Valley)
Blossom Hill (San Jose)
Coddingtown (Santa Rosa)
Franklin (San Francisco)
Potrero Hill (San Francisco)
South of Market (San Francisco)
Stanyan (San Francisco)
Stevens Creek (Cupertino)
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:
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
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.....
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:
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.
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.
Did I warn you that this was going to be a long one? Well, here goes -->
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 firstname.lastname@example.org.
Now your pet needs are also essential as veterinarian fees can be costly?
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.
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
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 :-(
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.
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.
Seafood Lovers....... pay attention!
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........
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 email@example.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.