Class II
Completed
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), Rx only, Distributed By Hospira, Inc., Lake Forest, IL 60045 USA,
This recall has been completed (originally issued January 11, 2023).
- Company
- Pfizer Inc.
- Recall Initiated
- December 29, 2022
- Posted
- January 11, 2023
- Recall Number
- D-0097-2023
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 62,088 bags
- Firm Location
- New York, NY, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Lack of assurance of sterility: Bags have the potential to leak.
Distribution
Nationwide in the USA.
Lot / Code Info
Lot: 5935283, Exp. 12/01/2023
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