Recall of Compounded Drugs Due to Sterility Issues
Read More
Recall - Due to N-Nitroso-Quinapril Content
Recall - Due to the Potential for a Missing Label in the Batch
Recall - Due to Presence of Methanol and Benzene
Recall - Due to the Presence of Undeclared Sildenafil
Class I Recall - Due to Risk of Falsely Low Results
Recall - Due to Presence of Slightly Elevated Levels of Benzene
Recall - Due to Presence of Particulate Matter
Recall - Due to Presence of Pluralibacter gergoviae
Recall - Due to Microbial Contamination
Recall - Due to N-NitrosoQuinapril Content
Recall - Due to Potential Manufacturing Defect
Recall - Due to Presence of a Nitrosamine Impurity
Class I Recall - Due to False Positive Test Results and Unauthorized Shelf Life
Class I Recall - Because Tests Are Not Authorized, Cleared, or Approved by the FDA and May Give False Results
Class I Recall - Because They Are Not Authorized, Cleared, or Approved by the FDA
A list of recent recalls on devices
Recall - Due to Presence of Methanol
Recall - Due to the Presence of Particulate Matter
Recall - Due to Fluid Leakage or Low Fill Volume
Class I Recall - Tests Not Authorized, Cleared, or Approved by the FDA and May Give False Results
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
Archives by Year