Complete FDA and NHTSA recall records dated in September 2018.
These records include useful source details for the selected month.
Medline notified BMD that the Aplicare Povidone Iodine (PVP-I) Prep Pads were not meeting the iodine assay level requirements to support 36 month expiration dating.
Ginger Spice Cookies are recalled because cookies may contain undeclared peanuts.
Iodized sea salt was packaged in Morton Natural Sea Salt packages.
FDA foreign inspection found pH levels in four products to be above their scheduled process.
Reports of off odor and off taste in Equate High Performance Protein Shake Chocolate led to recall of two lots of the product.
The product ingredients statement declares egg ingredients, but the "Contains" statement fails to declare egg.
Oatmeal Raisin Cookies are recalled because cookies may contain undeclared peanuts.
Don Froylan Requeson is being recalled because the ingredient statement does not declare milk, a major food allergen. The pasteurized whey comes from whole milk.
Potential contamination of Listeria monocytogenes
Chocolate Chip Cookies are recalled because cookies may contain undeclared peanuts.
FDA foreign inspection found pH levels in four products to be above their scheduled process.
Product is recalled due to undeclared milk. Sweetened Masala Chai boxes contain five single serve sachet packets of Chai Tea Latte, which declares milk, but Sweetened Masala Chai boxes do…
Foreign matter believed to be glass observed in retain samples of product.
FDA foreign inspection found pH levels in four products to be above their scheduled process.
FDA foreign inspection found pH levels in four products to be above their scheduled process.
Morgan Foods, Inc. initiated a voluntary recall of Tomato Condensed Soup, 26 oz. (1 LB 10 OZ) 737 g can, due to being mislabeled and containing cream of mushroom soup with undeclared…
Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
Failed Dissolution Specifications: manufacturer West-Ward Pharm Corp. recalled these repackaged lots due to failed dissolution results.
Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
Labeling Error: Not elsewhere classified. product has a dosage cup marked in teaspoons and the instructions on the label are described in milliliters.
Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
