Cardinal Health 200 PROTEXIS Latex Micro Surgical Gloves Size 7.0 - Product Usage: This recall — FDA Z-2915-2020
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
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.
Potential sterility issue
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.
Infusion pump component defect may result in interruption of patient monitoring
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…
Browse recent months with enough recall history for useful comparison.