Recalls

Class I Recall - Due to Distribution to U.S. Customers without Authorization, Clearance, or Approval from the FDA

Class I Recall - Risk of Misplaced Enteral Tubes Could Cause Patient Harm

Recall - Due to Microbial Contamination

Class I Recall - Due to Risk of False Positives Caused by Contamination

Recall of Compounded Drugs Due to Sterility Issues

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