Fossil Fuel Products, LLC, is voluntarily recalling lots QL110714A102 (20-count bottles) and QL110408B046 (single blister packs) of “RezzRX” to the consumer level.
Jobbers Wholesale Issues Voluntary Recall of Rhino 5 Plus, Maxtremezen and Extenzone Marketed as a Dietary Supplement Due to the Presence of Undeclared Drug Ingredients
Paramount, CA, Jobbers Wholesale is voluntarily recalling Lot No. KWAKPMC030505175957019 of Rhino 5 Plus, Lot No. JBP-L-1270-70 of Maxtremezen and Lot No. KWAKPMC03050517 of Extenzone to the consumer level. FDA analysis found these products to contain undeclared desmethylcarbondenafil and dapoxetine.
U.S. Marshals seize more than $2 million in adulterated dietary supplements from Georgia company
At the request of the U.S. Food and Drug Administration, U.S. Marshals seized dietary supplements manufactured and held by Hi-Tech Pharmaceuticals, Inc., located in Norcross, Ga., after FDA investigators found the products contained 1, 3-Dimethylamylamine HCl (DMAA) or its chemical equivalent. The retail value of the seized products is more than $2 million.
FDA Classifies Medtronic’s Worldwide Voluntary Field Action on Guidewires as Class I Recall
Medtronic, Inc. (NYSE: MDT) announced today that the U.S. Food and Drug Administration (FDA) has classified the company’s recently initiated voluntary field action related to certain guidewires as a Class I recall.
Based on an internal investigation following a limited number of complaints, including one patient injury, Medtronic began notifying hospitals and distributors worldwide the week of Oct. 21 that some models of its guidewires from recent lots have the potential for the coating on their surface to delaminate and detach.
New Reliance Traders, Inc.- Voluntarily Recalls Hashmi Surma Special Eyeliner Due to Elevated Lead Levels
New Reliance Traders, Inc announced it is voluntarily recalling all lots of Hashmi Surma Special Eyeliner because it was found to contain high levels of lead that could cause health problems to consumers, particularly infants, small children, and pregnant women.
La Boulange Cafe & Bakery Issues an Allergy Alert for Undeclared Allergen (Hazelnut) in Product Inadvertently Mislabeled as Soft Caramel Jam
La Boulange Cafe & Bakery voluntarily initiated a product recall of 75 Soft Caramel Jams in 8.4 oz. jars with lot number 822713 as a precautionary measure. This product was sold exclusively in 20 La Boulange Café & Bakery stores in the San Francisco Bay Area.
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Nature’s Pharmacy and Compounding Center Issues Voluntary Recall of All Sterile Compounded Products Distributed Within North Carolina Due to Lack of Sterility Assurance
ature’s Pharmacy and Compounding Center of Asheville, NC is voluntarily recalling of all lots of sterile products compounded by the pharmacy that are not expired to the consumer level. The product will be in the form of an injectable drug or an eye drop.
S&M Enterprise Issues Allergy Alert for Fruit of Wolfberry, 12 Oz Plastic Bag due to Undeclared Sulfites
S&M Enterprise of Bayonne, NJ is recalling all lots of Fruit of Wolfberry in 12 oz plastic bag packages. People who have allergies to sulfites run the risk of serious or life-threatening allergic reaction if they consume these products.
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FDA approves medical device to treat epilepsy
The U.S. Food and Drug Administration today approved a device to help reduce the frequency of seizures in epilepsy patients who have not responded well to medications.
Crunch Pak Issues Voluntary Recall of Limited Quantities of Crunch Pak Brand Apple Slices Because of Possible Health Risk
Crunch Pak of Cashmere, Washington is voluntarily recalling 5,471 cases of Crunch Pak Apple Slices due to a possible health risk from Listeria monocytogenes.