drugs MODERATE Updated 2025-08-27

PFIZER INC recalls Vial Label: 8.4% Sodium Bicarbonate Injection, USP, 50mEq/50

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Recalled 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.

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Hazard / Issue

Lack of Assurance of Sterility.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot #: LH2671, Exp. 11/30/2026

✅ What Should You Do?

  1. 1Stop taking this medication and contact your doctor or pharmacist immediately.
  2. 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
  3. 3Check the lot number on your bottle or packaging against the recalled lots listed above.
  4. 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.

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