Complete FDA and NHTSA recall records dated in 2020, 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.
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.
Multiple coatings of VITROS Chemistry Products AMYL Slides are showing imprecision on control fluids when compared to the expected within lab SD as listed on the Performance Verifier (PV)…
Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a different environmental oxygen level than what is displayed by the device, if a certain optional component…
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
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.
