FDAJune 17, 2020drug

Famotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only, Single Dose Vial, For Intravenous Use Only After Dilution, Distributed by HF Acquisition Co, LLC, Mukilteo, WA 98275, NDC 63323-739-12

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state.

What to do

FDA enforcement status: Terminated

Brands named

hf acquisition

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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