FDA recall record

Famotidine Injection, USP, 20 mg/2mL, 2 mL vial recall — FDA D-1392-2020

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

Class IIIclassification
D-1392-2020official record ID
Jul 29, 2020report date

Recall record at a glance

Official recordD-1392-2020
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmHF Acquisition Co. LLC
Report dateJul 29, 2020
Recall initiation dateJun 17, 2020
QuantityN/A
LocationMukilteo, WA, United States

Official product description

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

Why the product was recalled

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

Distribution information

The vials were distributed to one consignee located in CT.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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