Complete FDA and NHTSA recall records dated in September 2020.
These records include useful source details for the selected month.
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.
The Vantage Total Ankle Tibial Insert, Fixed Bearing, Size 4, Right 10mm, were found to have a labeling error. Exactech is recalling the Vantage Total Ankle Tibial Insert, Fixed Bearing,…
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.
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.
This letter is to inform you of the possibility that your Symbia S or Symbia T system(s) may have unintended slow motion of the detectors in specific situations which could pose a potential…
GEHC Surgery became aware that some users of the 9800 and 9900 fluoroscopic mobile C-Arms (referred to as the system here on) within the United States had requested that a Field Service…
Salsa products are recalled due to a potential contamination with Salmonella Newport. Onions were supplied from Thomson International, Inc
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
Potential contamination with Salmonella Newport in onions and prepared foods containing onions.
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
Undeclared lysozyme (from egg whites)
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
