Complete FDA and NHTSA recall records dated in 2021, 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.
Nissan North America, Inc. (Nissan) is recalling certain 2021 Rogue vehicles. The second-row upper tether wires may have been improperly welded to the seatback frame, preventing a child…
Specific lots may have been manufactured with insufficient or incomplete welds.
Specific lots may have been manufactured with insufficient or incomplete welds.
The component part numbers intended for shipment to a third-party, where they are further processed into kits and sterilized were instead shipped directly to customers.
Specific lots may have been manufactured with insufficient or incomplete welds.
Potential that a limited number of individual contact lens packages have an incomplete packaging seal.
Angio tubing included within Custom Convenience kits may contain insufficient or incomplete weld
Specific lots may have been manufactured with insufficient or incomplete welds.
Units from one batch of TriFit TS size 2 stem were found to be labeled as a TriFit CF size 7 stem. And vice versa.
Specific lots may have been manufactured with insufficient or incomplete welds.
Reports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.
Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.
Specific lots may have been manufactured with insufficient or incomplete welds.
The company was notified by their supplier of sterilization services for airway products in Italy of potential deviations from validated parameters for ethylene oxide sterilization.
Due to an issue with the internal clock of the analyzers with an e3800 PC unit installed.
Angio tubing included within Custom Convenience kits may contain insufficient or incomplete weld
Specific lots may have been manufactured with insufficient or incomplete welds.
Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventually detach from the baseplate, result in the display interface dismounting from…
Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.
Reports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.
Specific lots may have been manufactured with insufficient or incomplete welds.
Specific lots may have been manufactured with insufficient or incomplete welds.
Specific lots may have been manufactured with insufficient or incomplete welds.
Specific lots may have been manufactured with insufficient or incomplete welds.
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.
