Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
3M discovered that the Futuro" Quick Strap Ankle Brace (Cat. #47736EN) and ACE" Brand Deluxe Ankle brace (Cat. #207736) do not have the correct labeling. The products contain natural latex…
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is…
Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
Medtronic is voluntarily recalling one lot of its MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays, Lot 1717900160, following notification…
A limited portion of the lot was manufactured with less than the required amount of K2EDTA additive, an anticoagulant, which may cause erroneous results that could lead to specimen…
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is…
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is…
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is…
Contact lenses lack sterility assurance.
Certain models and lots of PORT A CATH implantable port kits may have been misassembled. The kits may incorrectly contain a 6Fr or 6.5Fr size introducer instead of the correct 8.5Fr size…
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Almond Love Bars are recalled due to undeclared soy lecithin.
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Firm is recalling Nut-Free Basil Pesto due to mislabeling, causing undeclared tree nuts.
Maple Minis are recalled due to undeclared soy lecithin.
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
The frozen waffle product contains whey but fails to declare the major food allergen "milk" on the label
9 inch Asparagus and Goat Cheese Quiche is recalled because egg is declared in the Ingredients statement but it is not declared in the Contains statement.
The firm is recalling the products listed below because it is mislabeled. Products labeled as Vegan Buffalo Chicken Bites are in fact Vegan Sonoma Chicken Salad. The label fails to declare…
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Customer notified firm after they received a positive result for Salmonella of Lot #90186-00 Cardamon Pods Green Whole Organic supplied by Starwest Botanicals
Browse recent months with enough recall history for useful comparison.
