Baxter Healthcare Corporation recalls Famotidine Injection in Sodium Chloride Injection, 20 mg, 50
See all recalls from Baxter Healthcare Corporation →Recalled 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.
Hazard / Issue
CGMP Deviations
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot # NC188586, Exp Date: 02/28/2027; Lot # NC188913, Exp Date: 3/9/2027.
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Famotidine Injection in Sodium →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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