FDAFDA · Food and drugs·Recall number D-1392-2020
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
Published July 29, 2020 · Recall initiated: June 17, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- FAMOTIDINE
- Manufacturer
- HF Acquisition Co. LLC
- Distributor
- The vials were distributed to one consignee located in CT.
- UPC
- 0363323739119
- Lot
- Lot #: 6122639, Exp. Date 08/2021
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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