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.
During an FDA investigation the firm was notified that the product contains undeclared milk.
Flour is declared but Wheat is not declared on label.
Undeclared milk allergen
During an FDA investigation the firm was notified that the product contains undeclared milk.
During an FDA investigation the firm was notified that the product contains undeclared milk.
Complaint received of foreign matter (metal) embedded in tablet.
Lack of Assurance of Sterility
Subpotent Drug: Out of specification for assay at the 30-month stability timepoint.
Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Menthol with UPC 7 14132 00071 4 instead of Peppermint Oil and Sage Oil with UPC 7 14132 00073 8
Lack of Assurance of Sterility
Microbial Contamination of Non-Sterile Products: presence of R. Pickettii bacteria
Defective Delivery System
A subset of affected discs are at risk of leakage when it is used more than one time with Simplexa COVID-19 Direct and/or Simplexa Flu A/B & RSV Direct Gen II. Leakage from a well that had…
There have been reports of stent migration.
(1)Software (SW) versions V1.25.1 and lower may result in TDef (Test Definition) Parameters for Open Channel Assays reverting to Default Value would shift test results by the magnitude of…
Mating incompatibility between the Inserter Shaft and the Inserter Draw Rod causing the inserter draw rod to bind and not rotate freely as intended surgeon may be unable to complete surgery…
Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the…
There is an issue with the installation of updated camera firmware on the system.
Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the…
There is a software defect that can cause the Amplification Detection clamp CLEAN position to be set too high.
There is a software issue associated with the ability to properly complete a Field Service Engineer Maintenance and Diagnostics procedure.
The dosage information on the pouch is incorrect; the primary carton label is correct.
There is a potential for abnormal (non-sigmoidal) amplification curves.
The current IFU specifies a shelf-life of one week after resuspension of the RPC Buffer when stored at room temperature. Ongoing stability studies have indicated the need to shorten the…
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.
