The Food and Drug Administration is advising consumers not to purchase or use Reumo Flex, a product promoted and sold for joint pain and arthritis on various websites, including https://botanical-be.com, and possibly in some retail stores. Read More (external link)...
Continue readingThe Food and Drug Administration is advising consumers not to purchase or use Tapee Tea, a product promoted and sold for pain relief on www.tapeeteausa.com, www.tapeetea.com, and possibly in some retail stores. Read More (external link)...
Continue readingThe Food and Drug Administration is advising consumers not to purchase or use Fast-Act Rheuma Capsule, a product promoted and sold for joint pain and rheumatoid arthritis on various websites and possibly in some retail stores. Read More (external link)...
Continue readingThis communication is part of the Communications Pilot to Enhance the Medical Device Recall Program Read More (external link)...
Continue readingFort Worth, Texas. Alcon Laboratories is voluntarily recalling one (1) lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101) to the consumer level. Alcon evaluated a consumer complaint of foreign material observed inside a sealed single use vial and determined th Read More (external link)...
Continue readingDECEMBER 20, 2024 – Lidl US is recalling all lots of their Taste of Deutschland Buttered Vegetables 10.5 oz box UPC 4 056489 122876 due to undeclared milk allergen. The recall was issued due to undeclared milk in the products. People who have allergies to milk run the risk of serious or life-threate Read More (external link)...
Continue readingEndo, Inc (OTCQX: NDOI) (“Endo”), announced today that one of its operating subsidiaries, Endo USA, Inc., is voluntarily recalling all lots within expiry of Adrenalin® Chloride Solution (EPINEPHrine nasal solution, USP) 30mg/30mL (1mg/mL) 30 mL vials, to the consumer level. This product, which pre-d Read More (external link)...
Continue readingJose Madrid Salsa is announcing a voluntary recall of our Chipotle Con Queso Salsa. The salsa is being recalled because it contains Yellow 5 and Yellow 6, which were not listed on the ingredient label. Individuals who are allergic or sensitive to Yellow 5 or Yellow 6 run the risk of minor to serious Read More (external link)...
Continue readingFDA-OCI, Phillip Jensen, Phillip M. Jensen, Springfield, Illinois, Rochester, Illinois Read More (external link)...
Continue readingThis communication is part of the Communications Pilot to Enhance the Medical Device Recall Program Read More (external link)...
Continue readingOrgain of Irvine, California is voluntarily recalling a single batch of its 30g Protein Organic Plant Based Powder - Chocolate 2.01lb because it may contain undeclared peanut residue. People who have an allergy or severe sensitivity to peanuts may run the risk of serious or life-threatening allergic Read More (external link)...
Continue readingFDA-OCI, Rahim Shafa, Novel Psychopharmacology Read More (external link)...
Continue readingFDA-OCI, Valley Processing Inc., Sunnyside, Washington, Mary Ann Bliesner Read More (external link)...
Continue readingFDA-OCI, Frankfort, Kentucky, Abigail Hall, Lawrenceburg, Kentucky Read More (external link)...
Continue readingBioZorb Markers are implantable and used to mark soft tissue for procedures. They are being recalled after reports of patient complications. Read More (external link)...
Continue readingDecember 16, 2024 – Los Angeles, California - Shoppers-Plaza is voluntarily recalling all lots of Fouzee Sugarlin Herbal Formula capsules to the consumer level. See Attachment 1 for photo of product labeling. Fouzee Sugarlin Herbal Formula capsules is an unapproved new drug for which safety and effi Read More (external link)...
Continue readingPOLARx Cryoablation Balloon Catheters treat atrial fibrillation. After reports of atrio-esophageal fistula, the use instructions are being updated. Read More (external link)...
Continue reading12/12/2024, Dover Plains, NY, GNMART INC is voluntarily recalling all lots of Force Forever for joint Pain, 60 Tablets packaged in a white plastic bottle with a red cap, labeled as "FORCE FOREVER.", to the consumer level. FDA analysis has found product to contain undeclared Diclofenac and Dexamethas Read More (external link)...
Continue readingThe FDA and CDC, in collaboration with state and local partners, are investigating a multistate outbreak of E. coli O157:H7 infections linked to raw milk cheese made by RAW FARM, LLC, of Fresno, CA. Read More (external link)...
Continue readingOutbreak Investigation of E. coli O157:H7: Bulk Organic Walnuts (April 2024) Read More (external link)...
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