Recall
FDAHealthAugust 4, 2025

PFIZER INC — 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.

⚠️ Lack of Assurance of Sterility.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
August 4, 2025

U.S. Nationwide

What's affected?

Product
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.
Lot code
LH2671

Additional details

Lot #: LH2671, Exp. 11/30/2026

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 15,750 vials.

View original FDA notice →

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