Jobbers Wholesale has recalled Lot No. KWAKPMC030505175957019 of Rhino 5 Plus, Lot No. JBP-L-1270-70 of Maxtremezen and Lot No. KWAKPMC03050517 of Extenzone after FDA analysis found these products to contain undeclared desmethylcarbondenafil and dapoxetine. Desmethylcarbondenafil is a phosphodiesterase PDE-5 inhibitor … Continued
Articles by The FDA
USPlabs LLC, of Dallas, TX has recalled all lots and sizes of the OxyElite Pro dietary supplements below. These products contain Aegeline, a synthesized version of a natural extract from the Bael tree. Epidemiological evidence shows that use of these … Continued
Tendex has recalled Lot# F51Q of P-Boost and Lot # F51Q of NatuRECT after FDA laboratory analysis on Lot# F51Q of P-Boost, which the firm also labels as NatuRECT, found that it contained undeclared tadalafil. Tadalafil is an active ingredient … Continued
CLR Medicals International Inc. is recalling Viscocel and Viscocel Plus. This drug recall is in response to FDA findings of deficiencies in the Quality System regulations for Medical Device Manufacturers, 21 Code of Federal Regulation (CFR) Part 820 and lack … Continued
Stryker Corporation (NYSE:SYK) announced today that its orthopaedic division has received notice that the U.S. Food and Drug Administration (FDA) has reviewed the voluntary recall of its ShapeMatch Cutting Guides and that it will be classified as a Class I … Continued
DZH Import & Export Inc. at 1300 Metropolitan Avenue, Brooklyn NY 11237 is recalling CURIOSITY OF DASHAN DRIED MUSHROOM because it contains undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions … Continued
Contact: Consumer: 1-800-800-4358 ext. 6 email@example.com Bunnell Incorporated has recalled Life Pulse High-Frequency Ventilator Patient Circuits. A complete list of Lot numbers affected by the recall is identified in the recall notice and on Bunnell’s website, www.bunl.com. The product has … Continued
True Taste, LLC of Kenosha, WI, is recalling it’s vacuum packaged Hot Smoked Rainbow Trout, Hot Smoked Whitefish, Hot Smoked Herring, Hot Smoked Mackerel, Hot Smoked Salmon Steak, Cold Smoked Mackerel, and Cold Smoked Whitefish because they have the potential … Continued
Contact: Consumer: 501-851-0002 Irma Harbour FOR IMMEDIATE RELEASE December 12, 2012 – The product in question is a single production run and packed in a 7.5 ounce paw print bag marked with a best by date of 08-2015. The best … Continued
Contact: Consumer: 1-800-444-4011 Media: Blaine Davis 1-610- 459-7158 FOR IMMEDIATE RELEASE December 6, 2012 – Qualitest, a subsidiary of Endo Health Solutions, (Nasdaq: ENDP) today issued a voluntary nationwide recall for 101 lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP … Continued
Salt Lake City, (GLOBE NEWSWIRE) – LifeVantage Corporation (NASDAQ: LFVN) announced today that it is contacting affected independent distributors and other customers to voluntarily recall and replace bottles of its Protandim®, the Nrf2 Synergizer®, dietary supplement from the lots shown … Continued
Lake Forest, Ill – Hospira, Inc. (NYSE: HSP), issued this press release today to further inform the general public about a previously communicated voluntary user-level recall of three lots of Carboplatin Injection due to visible particulates identified during a retain … Continued
Matrixx Initiatives is voluntarily recalling 1 lot of Zicam® Extreme Congestion Relief nasal gel. The company is taking this step after finding a small amount of Burkholderia cepacia in a single sample of the product taken from the affected lot. … Continued
Udi’s Healthy Foods, LLC of Denver, Colorado, is voluntarily recalling its 12-ounce bags of “Udi’s Gluten Free Au Naturel Granola” with UPC 6-98997-80615-8 and “Best By 041913 12265 1″ because they may contain undeclared almonds. People who are allergic to … Continued
Performance Plus Marketing, Inc. is recalling Libigrow®, Libigrow XXXtreme®, Blue Diamond®, Blue Diamond Platinum®, Mojo Nights®, Mojo Nights Supreme®, and Casanova® because they contain undeclared Sulfoaildenafil and Thioaildenafil.
P&J TRADING is conducting a voluntary nationwide recall of their dietary supplements sold under the brand name SLIMDIA REVOLUTION specific to the following product below. There is no identifying lot number.
Praxair, Inc. is in the process of conducting a voluntary recall involving Grab ‘n Go Vantage portable oxygen cylinder units. Praxair is making a minor modification to the affected units as they come in for routine servicing and filling. Praxair … Continued
Mylan Inc. announced that its Mylan Institutional business is recalling three lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/500 mg (Lots 3037841, 3040859 and 3042573).
Zimmer Spine, Inc. is initiating a voluntary worldwide recall of all 315 units of the PEEK Ardis® Inserter. The Ardis Inserter is a surgical instrument used during spinal surgery to implant the PEEK Ardis Interbody Spacer. The inserters are being … Continued
Mobius Therapeutics, LLC, St. Louis, MO, announced today that it is conducting a voluntary recall of 2 lots of Mitosol® (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use. The company is taking this voluntary action due to the fact … Continued