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.
A component issue may cause the AED to abort a shock delivery or reset unexpectedly, which may cause an affected device to fail to delivery shock, and/or to fail to deliver shock in range.
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020.
Undeclared major allergens (fish, egg, soy, milk, wheat, and crustacean shellfish) in "Captain Rusty's" brand Lobster Dip uncovered during FDACS routine inspection.
Undeclared major allergen (milk) in "Captain Rusty's" brand Smoked Salmon Dip uncovered during FDACS routine inspection.
Undeclared major allergens (fish, egg, soy, milk, wheat, and crustacean shellfish) in "Captain Rusty's" brand Cajun Crab & Lobster Dip uncovered during FDACS routine inspection.
Undeclared major allergens (fish, egg, soy, milk, and wheat) in "Captain Rusty's" brand Blue Crab Dip uncovered during FDACS routine inspection.
Undeclared major allergens (egg and soy) in "Captain Rusty's" brand Smoked Mahi Dip uncovered during FDACS routine inspection.
CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
Defective Container: Customer complaints received of a crimp defect while removing the flip-cap during use.
Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.
CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels
Defective Container: Customer complaints received of a crimp defect while removing the flip-cap during use.
CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
Superpotent Drug: The active ingredient, avobenzone, is used at 5% which is higher than the allowable 3% in the sunscreen formula per FDA sunscreen regulations.
CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
Subpotent Drug: Out-of-Specification potency results at the 30-day stability timepoint.
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2019-2020 RAV4 and 2020 RAV4 Hybrid vehicles equipped with electric power steering (EPS). Water may enter through the…
Distributed to the field without having completed design history files or design transfer activities
Distributed to the field without having completed design history files or design transfer activities
The recalling firm confirmed that SPA II and III users may encounter probes with unacceptable wear prior to reaching the 2500 piercings guideline indicated in the Instructions for Use…
Distributed to the field without having completed design history files or design transfer activities
There is potential for the plastic optical tip to become detached from the metal shaft.
The presence of N-acetyl-p-benzoquinone imine (NAPQI), a metabolite of acetaminophen, may cause interference in certain chemistry assays when testing patient samples.
Browse recent months with enough recall history for useful comparison.
