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.
Firm received sporadic reports of discoloration on certain lots of the product, which has been identified as common mold.
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
The reason for this field action is due to the mounting of a non-tamper-resistant (ordinary) battery drawer on some BABY440 hearing aids. The correct battery drawer is tamper-resistant and…
Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements per product specification for biological residues determined by LAL testing.
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
The seal of the sterile pouch may be compromised, thereby increasing the risk of infection.
Undeclared wheat and soy lecithin
Incorrect ingredients listed: Does not include Amaranth flour nor baking soda, but does include baking powder and vanilla
Undeclared wheat and soy lecithin
Undeclared wheat, soy lecithin, and milk
Product may contain undeclared milk.
Undeclared wheat, soy lecithin, and milk
Lloyd s Ice Cream of Evansville, IN is voluntarily recalling pre-packed quarts of Reese s Oreo Ice Cream because the product label does not declare peanuts.
Labeling: Not Elsewhere Classified: mislabeling of the Altavera generic name on the packaging component that may cause confusion.
Correct Labeled Product Mispack: confirmed report involving a single unit of properly labeled Heparin in 0.45% Sodium Chloride for Injection (NDC 0409-7651-03, Lot 87903FW) that was found…
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Discoloration: Presence of dark discoloration or brown spots on the edges of the tablets.
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Subpotent Drug: One lot of product does not meet the product specification for Assay test at 3 month long term stability condition.
Defective Delivery System: tablets may be missing, in whole or in part, the laser drilled holes on the metformin core of the Actoplus met XR tablets.
CGMP deviations
BMW of North America, LLC (BMW) is recalling certain 2019 BMW X5 xDrive40i vehicles. The capacitors within the Body Domain Controller (BDC) may short circuit and overheat.
Browse recent months with enough recall history for useful comparison.
