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All product recalls associated with PFIZER INC.
Total Recalls
148
Past Year
6
Class I (Serious)
22
Most Recent
Aug 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Lack of Assurance of Sterility.
Lack of Assurance of Sterility.
Subpotent drug
CGMP Deviations; particulates identified during visual inspection
CGMP Deviations; particulates identified during visual inspection
Discoloration; discolored solution from cracked vials
Lack of Assurance of Sterility-The potential for incomplete crimp seals.
Lack of Assurance of Sterility-The potential for incomplete crimp seals.
Presence of particulate matter: glass
Presence of Particulate Matter; identified as glass
Presence of Particulate Matter; identified as glass
Presence of Particulate Matter; identified as glass
Presence of Particulate Matter: identified as glass.
Presence of Particulate Matter: identified as glass.
Presence of Particulate Matter: identified as glass.
Labeling: Incorrect or Missing Lot and/or Exp Date: The carton and bottle labels state an expiry date of March 2026; the correct expiration date is February 2025.
Lack of assurance of sterility: Bags have the potential to leak.
Presence of Particulate Matter: Glass particulate matter detected in injectable.
Presence of Particulate Matter: A complaint was received for the presence of a hair in one vial.
Presence of particulate matter