Home / Recalls / Pfizer Inc. / D-0235-2024

D-0235-2024 Class I Ongoing

Recalled by Pfizer Inc. — New York, NY

Recall Details

Product Type
Drugs
Report Date
January 24, 2024
Initiation Date
December 21, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
24400 Cartons

Product Description

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, NDC 0409-4911-11 (carton), 0409-4911-34 (case).

Reason for Recall

Presence of Particulate Matter; identified as glass

Distribution Pattern

Nationwide in the USA and Puerto Rico.

Code Information

Lot GY2496, Exp 02/01/2025

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  • D-0489-2025 Class II — DOBUTamine Injection, USP, 250 mg/20 mL (12.5 mg/mL), 20 mL per Single-dose Vial (May 28, 2025)
  • D-0564-2024 Class II — Buprenorphine Hydrochloride Injection, 0.3 mg base/mL, 1 mL Single-dose Carpujec (May 20, 2024)
  • D-0565-2024 Class II — Labetalol Hydrochloride Injection, USP, 20 mg/4 mL (5 mg/mL), 4 mL Single-dose C (May 20, 2024)
  • D-0261-2024 Class I — Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop via (December 21, 2023)
  • D-0234-2024 Class I — 8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), Lifeshield, Gla (December 21, 2023)