Data Composite

Recall D-0809-2026

US Class II Ongoing · initiated 2026-08-06

Recalling firm

Baxter Healthcare Corporation, IL

Product

Famotidine Injection in Sodium Chloride Injection, 20 mg, 50 mL in GALAXY Single Dose Container, Rx Only, Sterile Nonpyrogenic, Baxter International Inc., Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-5197-41.

Reason for recall

CGMP Deviations

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