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

Date

2024-01-24

Country

United States

Brand

Pfizer

Product

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…

Classification

Class I

Units

Nationwide in the USA and Puerto Rico.

Category

Drugs & medical

Source

FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

1. Check the product name, strength and lot number against the official notice.
2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Pfizer recalls

1. 2025-07-02
2. US
   Drugs & medicalClass II

   Pfizer Inc. recalls 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…

   Discoloration; discolored solution from cracked vials

   FDA · DrugPfizer Inc.Nationwide in the USAOfficial notice →
3. 2024-07-03
4. 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 →
5. 2024-01-31
6. 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 →
7. 2023-11-15
8. 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 →
9. 2023-04-19
10. 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 →
11. 2023-02-01
12. 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 →

Other drugs & medical recalls in the United States

1. 2024-01-24
2. US
   Drugs & medicalClass I

   The Procter & Gamble Company recalls Secret, powder fresh, Aluminum chlorohydrate 24%, Anti-Perspirant/Deodorant, Topical spray can Net Wt., (a) 4OZ (113g), NDC…

   Chemical contamination: presence of benzene

   FDA · DrugThe Procter & Gamble CompanyNationwide USA and Puerto Rico, Canada, Guam, Northern Mariana Islands,…Official notice →
3. US
   Drugs & medicalClass II

   Ascend Laboratories, LLC recalls Ibuprofen and Famotidine Tablets 800mg/26.6mg, Rx Only, 90 Tablets per Bottle, manufactured by: Alkem Laboratories Ltd., INDIA,…

   Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet was discovered in an unopened bottle of Ibuprofen and Famotidine.

   FDA · DrugAscend Laboratories, LLCNationwideOfficial notice →
4. US
   Drugs & medicalClass I

   Insight Pharmaceuticals LLC, a Prestige Consumer… recalls Americaine, (benzocaine 20%) Benzocaine Topical Anesthetic Spray, Aerosol Can 2 oz (57 G), Dist. by Insight…

   Chemical Contamination: presence of benzene

   FDA · DrugInsight Pharmaceuticals LLC, a Prestige Consumer…Nationwide in the USAOfficial notice →
5. US
   Drugs & medicalClass II

   Par Sterile Products LLC recalls Vasostrict (vasopressin in 5% Dextrose) Injection, 20 units per 100 mL (0.2 units per mL), 100 mL x 10 Single Dose Vials per carton,…

   Superpotent Drug: Assay from the 3-month and 6-month stability intervals exceeded the upper specification limit.

   FDA · DrugPar Sterile Products LLCNationwide USAOfficial notice →
6. US
   Drugs & medicalClass II

   Pharma Nobis LLC recalls Freskaro refresh & revitalize Magnesium Citrate Saline Laxative Oral Solution Grape Flavor 10 fl. oz, Manufactured by: Pharma Lobis, 7400…

   MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.

   FDA · DrugPharma Nobis LLCNationwide.Official notice →
7. 2024-01-17
8. US
   Drugs & medicalClass II

   Philips North America recalls (1) Ingenia Ambition X (Product Number 781356); (2) Ingenia Ambition S (Product Number 781359)

   The sealed magnet will experience uncontrolled shutdown known as Loss-of-Field (LoF) if the magnet loses cryo-cooling (e.g. caused by a power outage on site.)

   FDA · DevicePhilips North AmericaDomestic distribution to the following states and territories: CA DE FL GA IL…Official notice →