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
Reported: July 29, 2020 Initiated: June 17, 2020 #D-1392-2020
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
Reason for Recall
TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state.
Details
- Recalling Firm
- HF Acquisition Co. LLC
- Units Affected
- N/A
- Distribution
- The vials were distributed to one consignee located in CT.
- Location
- Mukilteo, WA
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by HF Acquisition Co. LLC. Units affected: N/A.
Why was this product recalled? ▼
TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 29, 2020. Severity: Low. Recall number: D-1392-2020.
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