Drug recall D-1392-2020
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
Reason for recall
TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state.
Lots and codes
Lot #: 6122639, Exp. Date 08/2021
Recall details
- Recalling firm
- HF Acquisition Co. LLC, Mukilteo, WA
- Quantity
- N/A
- Distribution
- The vials were distributed to one consignee located in CT.
- Type
- Voluntary: Firm initiated
- Recall initiated
- June 17, 2020
- Terminated
- April 13, 2021
Related products
- Famotidine – drug information
- NDC 63323-739 Famotidine · Famotidine 10 mg/mL · Fresenius Kabi USA, LLC