Class I Recall - Tests Not Authorized, Cleared, or Approved by the FDA and May Give False Results
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Recall - Due to Possible Presence of Cronobacter sakazakii, Salmonella Newport
Class I Recall - May Give False Results and Require Special Training for Safe Handling
Recall - Due to Presence of Benzene
Recall - Due to the Presence of Undeclared Tadalafil
Recall - Due to the Presence of Undeclared Sildenafil and Tadalafil
Recall - Due to Test Kits Being Illegally Imported Into The United States
Recall - Due to the Presence of Tadalafil
Recall - Due to the Presence of Particulate Matter
Recall - Due to Bacterial Contamination
Class I Recall - Due to a Risk of Harmful Chemical Exposure
Recall - Due to the Potential for a Missing Label in the Batch
Recall - Due to Microbial Contamination
Recall - Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity
Recall - Due to Possible Health Risk
Class I Recall - Due to Reports of Fluid Leaks
Recalls involving N-Nitrosodimethylamine (NDMA) content.
Recall - Due to a Possible Defective Delivery System
Recall Due to Presence of Glass Particulates
Recall Expansion - Due to Microbial Contamination Concerns
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