HF Acquisition Co. LLC recalls Famotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only, Single Dose Vial, For Intravenous Use Only After Dilution, Dis
Recalled July 29, 2020 · FDA recall D-1392-2020 · HF Acquisition
Hazard
TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state. · FDA Class III
Units
N/A
Sold at
The vials were distributed to one consignee located in CT.
Description
TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state.
Product
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
Manufacturer(s)
HF Acquisition Co. LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →