--- title: "Pfizer Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Pfizer Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/pfizer-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Pfizer Inc. recall records **11** reported ongoing 31 records in this archive. Latest source date Aug 4, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 4, 2025 FDA drug enforcement ### [Vial Label: Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045, USA. NDC 0409-4933-05. Case: NDC 0409-4933-10.](https://isitonrecall.com/recall/fda-drug-d-0590-2025-vial-label-epinephrine-injection-usp-1mg-10ml-0-1-mg-ml-rx-only-distributed-by-hospira-inc-lake-fore/) Lack of Assurance of Sterility. Class II Reported ongoing Distribution: U.S. Nationwide [Official source for Vial Label: Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL), Rx only, Distributed by Hospira, In...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0590-2025%22) Aug 4, 2025 FDA drug enforcement ### [Vial Label: 8.4% Sodium Bicarbonate Injection, USP, 50mEq/50 mL (1 mEq/mL), Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-6637-24. Case NDC: 00409-6637-14.](https://isitonrecall.com/recall/fda-drug-d-0591-2025-vial-label-8-4-sodium-bicarbonate-injection-usp-50meq-50-ml-1-meq-ml-rx-only-hospira-inc-lake-forest/) Lack of Assurance of Sterility. Class II Reported ongoing Distribution: U.S. Nationwide [Official source for Vial Label: 8.4% Sodium Bicarbonate Injection, USP, 50mEq/50 mL (1 mEq/mL), Rx only, Hospira, Inc...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0591-2025%22) Jul 10, 2025 FDA drug enforcement ### [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 York, NY 10001. Made in Austria, Carto...](https://isitonrecall.com/recall/fda-drug-d-0544-2025-bicillin-l-a-penicllin-g-benzathine-injectable-suspension-1-200-000-units-per-2-ml-2-ml-vial-rx-only/) CGMP Deviations; particulates identified during visual inspection Class II Reported ongoing Distribution: Nationwide in the USA [Official source for Bicillin L-A (penicllin G benzathine injectable suspension), 1,200,000 units per 2 mL, 2 mL-vial,...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0544-2025%22) Jul 10, 2025 FDA drug enforcement ### [Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001, Made in Austria, Carto...](https://isitonrecall.com/recall/fda-drug-d-0545-2025-bicillin-l-a-penicillin-g-benzathine-injectable-suspension-2-400-000-units-per-4-ml-4ml-vial-rx-only/) CGMP Deviations; particulates identified during visual inspection Class II Reported ongoing Distribution: Nationwide in the USA [Official source for Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial,...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0545-2025%22) May 28, 2025 FDA drug enforcement ### [DOBUTamine Injection, USP, 250 mg/20 mL (12.5 mg/mL), 20 mL per Single-dose Vial, carton of 10 Fliptop Vials, Rx only, For Intravenous Use Only, Made in Italy, Distributed by Ho...](https://isitonrecall.com/recall/fda-drug-d-0489-2025-dobutamine-injection-usp-250-mg-20-ml-12-5-mg-ml-20-ml-per-single-dose-vial-carton-of-10-fliptop-via/) Discoloration; discolored solution from cracked vials Class II Reported ongoing Distribution: Nationwide in the USA [Official source for DOBUTamine Injection, USP, 250 mg/20 mL (12.5 mg/mL), 20 mL per Single-dose Vial, carton of 10 Fl...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0489-2025%22) May 20, 2024 FDA drug enforcement ### [Buprenorphine Hydrochloride Injection, 0.3 mg base/mL, 1 mL Single-dose Carpuject, Sterile Cartridge Unit with Luer Lock, For Intramuscular or Intravenous Use, Rx Only, Distribu...](https://isitonrecall.com/recall/fda-drug-d-0564-2024-buprenorphine-hydrochloride-injection-0-3-mg-base-ml-1-ml-single-dose-carpuject-sterile-cartridge-un/) Lack of Assurance of Sterility-The potential for incomplete crimp seals. Class II Reported ongoing Distribution: US Nationwide and Puerto Rico. [Official source for Buprenorphine Hydrochloride Injection, 0.3 mg base/mL, 1 mL Single-dose Carpuject, Sterile Cartri...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0564-2024%22) May 20, 2024 FDA drug enforcement ### [Labetalol Hydrochloride Injection, USP, 20 mg/4 mL (5 mg/mL), 4 mL Single-dose Carpuject, Sterile Cartridge Unit with Luer Lock, For Intravenous Injection Only, Rx Only, Distrib...](https://isitonrecall.com/recall/fda-drug-d-0565-2024-labetalol-hydrochloride-injection-usp-20-mg-4-ml-5-mg-ml-4-ml-single-dose-carpuject-sterile-cartridg/) Lack of Assurance of Sterility-The potential for incomplete crimp seals. Class II Reported ongoing Distribution: US Nationwide and Puerto Rico. [Official source for Labetalol Hydrochloride Injection, USP, 20 mg/4 mL (5 mg/mL), 4 mL Single-dose Carpuject, Sterile...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0565-2024%22) Dec 21, 2023 FDA drug enforcement ### [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 Syringe per Carton, Hospira, Inc., Lake ...](https://isitonrecall.com/recall/fda-drug-d-0233-2024-4-2-sodium-bicarbonate-injection-usp-5-meq-10-ml-0-5-meq-ml-glass-abboject-unit-of-use-syringe-for-i/) Presence of Particulate Matter; identified as glass Class I Reported ongoing Distribution: Nationwide in the USA and Puerto Rico. [Official source for 4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syrin...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0233-2024%22) Dec 21, 2023 FDA drug enforcement ### [8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 50 mL Syringe per Carton, Hospira, Inc., Lake Forest, I...](https://isitonrecall.com/recall/fda-drug-d-0234-2024-8-4-sodium-bicarbonate-injection-usp-50-meq-50-ml-1-meq-ml-lifeshield-glass-abboject-unit-of-use-syr/) Presence of Particulate Matter; identified as glass Class I Reported ongoing Distribution: Nationwide in the USA and Puerto Rico. [Official source for 8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), Lifeshield, Glass ABBOJECT Unit ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0234-2024%22) Dec 21, 2023 FDA drug enforcement ### [Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake FOrest, IL 60045, ...](https://isitonrecall.com/recall/fda-drug-d-0235-2024-atropine-sulfate-injection-usp-1-mg-10-ml-0-1-mg-ml-lifeshield-glass-abboject-unit-of-use-syringe-rx/) Presence of Particulate Matter; identified as glass Class I Reported ongoing Distribution: Nationwide in the USA and Puerto Rico. [Official source for Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of Use Sy...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0235-2024%22) Oct 2, 2023 FDA drug enforcement ### [4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5mEq/mL), Glass ABBOJECT Unit of Use Syringe, packaged as 1 vial and injector per carton, Rx only, Hospira Inc., Lake Fores...](https://isitonrecall.com/recall/fda-drug-d-0100-2024-4-2-sodium-bicarbonate-injection-usp-5-meq-10-ml-0-5meq-ml-glass-abboject-unit-of-use-syringe-packag/) Presence of Particulate Matter: identified as glass. Class I Reported terminated Distribution: Nationwide in the US and Puerto Rico. The products were not distributed to government accounts or foreign consignees. [Official source for 4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5mEq/mL), Glass ABBOJECT Unit of Use Syring...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0100-2024%22) Oct 2, 2023 FDA drug enforcement ### [1% Lidocaine HCl Injection, USP, 50mg/5mL(10mg/mL), Glass ABBOJECT Unit of Use Syringe, packaged as 1 vial and injector per carton, Rx only, Distributed by Hospira Inc., Lake Fo...](https://isitonrecall.com/recall/fda-drug-d-0101-2024-1-lidocaine-hcl-injection-usp-50mg-5ml-10mg-ml-glass-abboject-unit-of-use-syringe-packaged-as-1-vial/) Presence of Particulate Matter: identified as glass. Class I Reported terminated Distribution: Nationwide in the US and Puerto Rico. The products were not distributed to government accounts or foreign consignees. [Official source for 1% Lidocaine HCl Injection, USP, 50mg/5mL(10mg/mL), Glass ABBOJECT Unit of Use Syringe, packaged ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0101-2024%22) Oct 2, 2023 FDA drug enforcement ### [2% Lidocaine HCl Injection, USP, 100mg/5mL(20mg/mL), Glass ABBOJECT Unit of Use Syringe, packaged as 1 vial and injector per carton, Rx only, Distributed by Hospira Inc., Lake F...](https://isitonrecall.com/recall/fda-drug-d-0102-2024-2-lidocaine-hcl-injection-usp-100mg-5ml-20mg-ml-glass-abboject-unit-of-use-syringe-packaged-as-1-via/) Presence of Particulate Matter: identified as glass. Class I Reported terminated Distribution: Nationwide in the US and Puerto Rico. The products were not distributed to government accounts or foreign consignees. [Official source for 2% Lidocaine HCl Injection, USP, 100mg/5mL(20mg/mL), Glass ABBOJECT Unit of Use Syringe, packaged...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0102-2024%22) Mar 8, 2023 FDA drug enforcement ### [MEKTOVI (binimetinib) tablets, 15 mg, 180-count bottle, Rx only, Distributed by: Array BioPharma Inc., a wholly owned subsidiary of Pfizer Inc., Boulder, CO 80301. NDC: 70255-01...](https://isitonrecall.com/recall/fda-drug-d-0532-2023-mektovi-binimetinib-tablets-15-mg-180-count-bottle-rx-only-distributed-by-array-biopharma-inc-a-whol/) 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. Class III Reported ongoing Distribution: Nationwide in the USA [Official source for MEKTOVI (binimetinib) tablets, 15 mg, 180-count bottle, Rx only, Distributed by: Array BioPharma ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0532-2023%22) Dec 29, 2022 FDA drug enforcement ### [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 0409-7620-59), b) Single Unit (NDC 0409-7620-49), R...](https://isitonrecall.com/recall/fda-drug-d-0097-2023-heparin-sodium-2-000-usp-units-per-1-000-ml-2-usp-units-ml-in-0-9-sodium-chloride-injection-1-000-ml/) Lack of assurance of sterility: Bags have the potential to leak. Class II Reported completed Distribution: Nationwide in the USA. [Official source for Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection,...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0097-2023%22) Dec 22, 2022 FDA drug enforcement ### [Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop Vial, 10 vials per carton, Rx only, Distributed by: Hospira, Inc., Lake Forest, IL 6...](https://isitonrecall.com/recall/fda-drug-d-0184-2023-vancomycin-hydrochloride-for-injection-usp-1-5-g-vial-sterile-powder-single-dose-fliptop-vial-10-via/) Presence of Particulate Matter: Glass particulate matter detected in injectable. Class I Reported terminated Distribution: USA nationwide and Puerto Rico [Official source for Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop Vial...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0184-2023%22) Sep 27, 2022 FDA drug enforcement ### [Aminophylline Injection, USP 250 mg/10 mL (25 mg/mL) 25x10 mL Single-dose vial, Rx only, Distributed by Hospira, Inc. Lake Forest, IL 60045 USA. NDC 0409-5921-16 (vial) 0409-592...](https://isitonrecall.com/recall/fda-drug-d-0003-2023-aminophylline-injection-usp-250-mg-10-ml-25-mg-ml-25x10-ml-single-dose-vial-rx-only-distributed-by-h/) Presence of Particulate Matter: A complaint was received for the presence of a hair in one vial. Class II Reported terminated Distribution: Distributed in the United States and Puerto Rico. [Official source for Aminophylline Injection, USP 250 mg/10 mL (25 mg/mL) 25x10 mL Single-dose vial, Rx only, Distribu...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0003-2023%22) Aug 22, 2022 FDA drug enforcement ### [PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL glass fliptop vial (NDC 0409-4699-54) further packaged in a tray of 10 vials (NDC Carton: 0409-4699-24), ...](https://isitonrecall.com/recall/fda-drug-d-1540-2022-propofol-injectable-emulsion-1-g-100-ml-10-mg-ml-packaged-in-100-ml-glass-fliptop-vial-ndc-0409-4699/) Presence of particulate matter Class I Reported terminated Distribution: USA Nationwide [Official source for PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL glass fliptop vial (NDC 0...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1540-2022%22) Jul 13, 2022 FDA drug enforcement ### [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 tray of 10 vials (NDC Carton: 0409-4699-2...](https://isitonrecall.com/recall/fda-drug-d-1301-2022-propofol-injectable-emulsion-1-g-100-ml-10-mg-ml-packaged-in-100-ml-per-glass-fliptop-vial-ndc-0409/) Presence of particulate matter: particulate identified as a beetle. Class I Reported terminated Distribution: USA Nationwide [Official source for Propofol Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL per glass fliptop vial (N...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1301-2022%22) Apr 22, 2022 FDA drug enforcement ### [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](https://isitonrecall.com/recall/fda-drug-d-0872-2022-accupril-quinapril-hcl-tablets-10-mg-90-tablets-rx-only-ndc-0071-0530-23-distributed-by-parke-davis/) CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits. Class II Reported terminated Distribution: Nationwide and Puerto Rico [Official source for Accupril (Quinapril HCl Tablets) 10 mg, 90 Tablets Rx only NDC 0071-0530-23 Distributed by: Parke...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0872-2022%22) ## Reasons in these listed records - Lack of Assurance of Sterility. - CGMP Deviations; particulates identified during visual inspection - Discoloration; discolored solution from cracked vials - Lack of Assurance of Sterility-The potential for incomplete crimp seals. These examples come from this result page and are not a ranking of every recall reason. ## Checking Pfizer Inc. ### Is there a recall on pfizer inc. right now? This archive contains 31 records, including 11 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Pfizer Inc.](https://isitonrecall.com/check/?q=Pfizer%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)