Class I Recall - Due to Risk of Falsely Low Results
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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
Archives by Year
