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.
World Flavors, Inc. initiated a recall of 085-CH-550-35 Cheese Whiz-Small Bag-No Art. Colors Lots 9280009, 9280010, 9280011, 9280012 and 025-BBQ-468 Barbeque Sauce Base Lot 9283079, because…
Potential Listeria monocytogenes contamination of Butternut Squash
Wild Harvest Organic Basil has the potential to be contaminated with Cyclospora cayetanensis.
Product contained an ingredient (farro) that potentially contain small stones.
World Flavors, Inc. initiated a recall of 085-CH-550-35 Cheese Whiz-Small Bag-No Art. Colors Lots 9280009, 9280010, 9280011, 9280012 and 025-BBQ-468 Barbeque Sauce Base Lot 9283079, because…
Failed dissolution specification - dissolution results of 59% (spec. NLT 85%) at the 24 month time point (end of shelf life).
Presence of Particulate Matter: particulate matter identified after reconstitution.
Presence of Particulate Matter - found in reserve sample vials at the firm.
Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.
Subpotent drug - Product did not contain drug.
Failed Impurities/Degradation Specifications: potential migration of benzophenone at very low level into the product from container.
Presence of Particulate Matter - found in reserve sample vials at the firm.
BMW of North America, LLC (BMW) is recalling certain 2019 Z4 sDrive30i, 2019-2020 330i xDrive, M340i and M340i xDrive, 2020 X3M and X4M, and Toyota Supra vehicles. In certain driving…
Mazda North American Operations (Mazda) is recalling certain 2020 CX-30 vehicles equipped with all-wheel drive. The evaporative vent hose for the fuel tank may be disconnected, possibly…
Mazda North American Operations (Mazda) is recalling certain 2020 CX-30 and Mazda3 vehicles. The front brake caliper mounting bolts may not have been tightened properly during assembly,…
The surgical gowns were manufactured in a facility that is not registered by the FDA.
The Pressure Monitoring Set and Tray may contain excess coating material on the outside and/or interior of the needle component which could cause occlusion.
After the device has been in use for about 2 months, data processing in the PDM can be slowed such that the Bolus Calculator fails to accurately subtract the correct amout of IOB before…
There are reports of inadequate locking of the extended tab screws. Complaints were reported where the closure top backed out of the screw post-operatively.
There are reports of inadequate locking of the extended tab screws. Complaints were reported where the closure top backed out of the screw post-operatively.
Packaged dental implant healing abutments were found to contain the wrong size device.
In the case of an AQM clot detection error a portion of the distilled water from the Aliquoter Module hydraulic circuit may be dispensed into the Primary Tube leading to sample dilution,…
There are reports of inadequate locking of the extended tab screws. Complaints were reported where the closure top backed out of the screw post-operatively.
The labeling of the Philips Chest Pneumograph does not include a statement indicating that the product contains natural rubber latex.
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.
