Pfizer recalls

18 official recalls and safety alerts involving Pfizer since 2021-12, from FDA · Drug. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Pfizer or the relevant agency.

  1. 2026-09-23
  2. US
  3. 2025-08-27
  4. US
  5. 2025-08-20
  6. US
  7. 2025-08-06
  8. US
    Drugs & medicalClass II

    Pfizer Inc. recalls Bicillin L-A (penicllin G benzathine injectable suspension), 1,200,000 units per 2 mL, 2 mL-vial, Rx Only, Distributed by Pfizer Inc., New…

    CGMP Deviations; particulates identified during visual inspection

    FDA · DrugPfizer Inc.Nationwide in the USAOfficial notice →
  9. 2025-07-02
  10. US
  11. 2024-07-03
  12. US
    Drugs & medicalClass II

    Pfizer Inc. recalls Labetalol Hydrochloride Injection, USP, 20 mg/4 mL (5 mg/mL), 4 mL Single-dose Carpuject, Sterile Cartridge Unit with Luer Lock, For…

    Lack of Assurance of Sterility-The potential for incomplete crimp seals.

    FDA · DrugPfizer Inc.US Nationwide and Puerto Rico.Official notice →
  13. 2024-01-31
  14. US
    Drugs & medicalClass I

    PFIZER recalls Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop vial, Rx Only, Distributed by: Hospira, Inc., Lake Forest, IL…

    Presence of particulate matter: glass

    FDA · DrugPFIZERNationwide in the USA, Netherlands and LibyaOfficial notice →
  15. 2024-01-24
  16. US
    Drugs & medicalClass I

    Pfizer Inc. recalls 4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous Use, Rx Only, 10 mL…

    Presence of Particulate Matter; identified as glass

    FDA · DrugPfizer Inc.Nationwide in the USA and Puerto Rico.Official notice →
  17. 2023-11-15
  18. US
    Drugs & medicalClass I

    Pfizer Inc. recalls 2% Lidocaine HCl Injection, USP, 100mg/5mL(20mg/mL), Glass ABBOJECT Unit of Use Syringe, packaged as 1 vial and injector per carton, Rx…

    Presence of Particulate Matter: identified as glass.

    FDA · DrugPfizer Inc.Nationwide in the US and Puerto Rico. The products were not distributed to…Official notice →
  19. 2023-04-19
  20. US
    Drugs & medicalClass III

    Pfizer Inc. recalls MEKTOVI (binimetinib) tablets, 15 mg, 180-count bottle, Rx only, Distributed by: Array BioPharma Inc., a wholly owned subsidiary of Pfizer…

    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.

    FDA · DrugPfizer Inc.Nationwide in the USAOfficial notice →
  21. 2023-02-01
  22. US
    Drugs & medicalClass I

    Pfizer Inc. recalls Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop Vial, 10 vials per carton, Rx only,…

    Presence of Particulate Matter: Glass particulate matter detected in injectable.

    FDA · DrugPfizer Inc.USA nationwide and Puerto RicoOfficial notice →
  23. 2023-01-11
  24. US
    Drugs & medicalClass II

    Pfizer Inc. recalls Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection, 1,000 mL bags, a) Case (NDC…

    Lack of assurance of sterility: Bags have the potential to leak.

    FDA · DrugPfizer Inc.Nationwide in the USA.Official notice →
  25. 2022-10-12
  26. US
    Drugs & medicalClass II

    Pfizer Inc. recalls Aminophylline Injection, USP 250 mg/10 mL (25 mg/mL) 25x10 mL Single-dose vial, Rx only, Distributed by Hospira, Inc. Lake Forest, IL…

    Presence of Particulate Matter: A complaint was received for the presence of a hair in one vial.

    FDA · DrugPfizer Inc.Distributed in the United States and Puerto Rico.Official notice →
  27. 2022-09-21
  28. US
  29. 2022-08-03
  30. US
    Drugs & medicalClass I

    Pfizer Inc. recalls Propofol Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL per glass fliptop vial (NDC 0409-4699-54) further packaged in a…

    Presence of particulate matter: particulate identified as a beetle.

    FDA · DrugPfizer Inc.USA NationwideOfficial notice →
  31. 2022-05-25
  32. US
    Drugs & medicalClass II

    Pfizer Inc. recalls Accupril (Quinapril HCl Tablets) 10 mg, 90 Tablets Rx only NDC 0071-0530-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017

    CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.

    FDA · DrugPfizer Inc.Nationwide and Puerto RicoOfficial notice →
  33. 2022-04-13
  34. US
    Drugs & medicalClass II

    Pfizer Inc. recalls quinapril and hydrochlorothiazide tablets, 20 mg/25 mg*, 90 Tablets bottles, Rx Only, Distributed by: Greenstone, LLC, Peapack, NJ, 07977,…

    CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.

    FDA · DrugPfizer Inc.NationwideOfficial notice →
  35. 2021-12-08
  36. US
    Drugs & medicalClass II

    Pfizer Inc. recalls 5% Dextrose Injection, USP, 50 mL ADD-Vantage Unit, Rx only, Distributed by Hospira, INC., Lake Forest, IL 60045 USA, NDC…

    Lack of sterility assurance: bag has the potential to leak.

    FDA · DrugPfizer Inc.USA NationwideOfficial notice →