Complete FDA and NHTSA recall records dated in 2018, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
On systems equipped with the Auxiliary Common Gas Outlet (ACGO), there is a potential for the auxiliary gas switch to unexpectedly switch from the ACGO position back to the circle position.…
When attempting to recapture the 32-mm device, the tip of the delivery sheath may fold or buckle, resulting in increased retraction force and difficulty or failure to recapture the device.
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.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
