Safety alertSource: FDA Drug Enforcement Reports

Class II recall: Baxter Healthcare Corporation: Famotidine Injection in Sodium Chloride Injection, 20 mg, 50 mL in GALAXY Single

Baxter Healthcare Corporation has issued a Class II recall for Famotidine Injection in Sodium Chloride Injection (20 mg/50 mL) supplied in GALAXY Single Dose Containers, NDC 0338-5197-41. The recall notice cites current Good Manufacturing Practice (CGMP) deviations as the reason for the action; no further clinical details were provided in the source.

Most relevant for: Hospital and inpatient care settings using intravenous famotidine, including gastroenterology services managing acid-related conditions requiring parenteral H2-receptor antagonist therapy.

Read the original at FDA Drug Enforcement Reports

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Informational only. Not medical advice. Not a substitute for clinical judgment. Always consult current guidelines and your own clinical judgment.

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