Complete FDA and NHTSA recall records dated in 2022, 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.
Ford Motor Company (Ford) is recalling certain 2020 Escape and 2021 Lincoln Corsair vehicles equipped with 2.5L hybrid powertrains. Insufficient welds inside the high voltage battery may…
Ford Motor Company (Ford) is recalling certain 2022 Mustang vehicles equipped with an Image Processing Module A (IPMA) or forward-facing camera. The camera is misaligned to the vehicle,…
Chryler (FCA US, LLC) is recalling certain 2022 Jeep Wrangler vehicles. The side marker lights may not function due to an incompatible tail light assembly wiring harness. As such, these…
In the Azurion system, the user can add a new study to a patient by selecting the option Add Study . The Add Study dialogue box is then displayed where the Patient Type is selected to…
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
The product was distributed without FDA authorization or clearance for marketing and distribution in the US.
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
During re-work of disposable instruments to relabel for 4-year shelf-life of disposable instruments, parts got mixed into other lots.
Product labeled incorrectly. The lot was labeled with Small footprint when the product was Medium.
System software v1.5.1 has a system software issue related to the Daylight Savings Time (DST) change that can cause a system error, requiring the user to restart the system and potentially…
When updating BD Kiestra customers to BD Synapsys version 4.10, the custom antibiotic codes set by the customer are overwritten with the BD default antibiotic codes.
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
During re-work of disposable instruments to relabel for 4-year shelf-life of disposable instruments, parts got mixed into other lots.
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
Potential breach in the sterility barrier for tray ring covers.
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
There is a potential for foreign matter.
Potential to contain undeclared wheat and whey
Product contains undeclared sulfites and unallowed dye - Amaranth (E123) - Acid Red 27
Product contains undeclared sulfites.
Product contains undeclared sulfites.
Possible Listeria monocytogenes in product
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
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.
