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.
CGMP deviations; there is a possibility that some bottles in these lots may have the active ingredient above and/or below specification limits.
Ford Motor Company (Ford) is recalling certain 2019-2020 Edge, Transit Connect and Lincoln MKX and 2020 Escape and Lincoln Corsair vehicles. The start/stop accumulator endcap may have…
Ford Motor Company (Ford) is recalling certain 2020 Explorer vehicles. The affected vehicles are equipped with second row center seat belt buckles that may not be properly secured to the…
Chrysler (FCA US LLC) is recalling certain 2020 Jeep Gladiator and Jeep Cherokee, 2019-2020 Ram 1500 Pickup, Ram 2500 Pickup, Ram 3500 Pickup, Chrysler Pacifica, Dodge Durango, Jeep Grand…
Sample leaking from the sleeve covering the needle inside the cannula
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
Amylase AY3805 batch 480449 and Pancreatic Amylase AY3855 batch 480483 have failed to meet the quoted performance claims prior to expiry on 28th Sept 2020.
Potential sterility issue
The product contains a non-functional component not referenced in product labeling.
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
Infusion pump component defect may result in interruption of patient monitoring
The product contains a non-functional component not referenced in product labeling.
The product contains a non-functional component not referenced in product labeling.
Holding force of the Positioning Arm can be reduced by prolonged non-use.
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
The connector linking the EtCO2 module to the HemoBox may break and become damaged, if the connector is re-attached to the HemoBox in this damaged state, under certain incorrect pin…
Thermo Scientific" Remel" Bordetella pertussis Agglutinating Serum (R30165501/ZM10) is not performing, resulting in the potential for false negative results for serotypes 1 and 3
Dimension Vista High Sensitivity Troponin I (TNIH) may exhibit a negative bias with patient samples
The product contains a non-functional component not referenced in product labeling.
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
The product contains a non-functional component not referenced in product labeling.
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.
