Reported Jul 29, 2020 · Terminated

Famotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only, Single Dose Vial, For Intravenous Use Only After Dilution,…

HF Acquisition Co. LLC

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: HF Acquisition Co. LLC · 11629 49th Pl W · Mukilteo, WA · 98275-4255

Is this the product you have?

  • 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
Lot codes and dates
    • Lot #: 6122639
    • Exp. Date 08/2021
Amount recalled
N/A

Where it was sold

Why it was recalled

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

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Apr 13, 2021 · Data as of Sep 19, 7:20 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.