Drug recall
Famotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only, Single Dose Vial, For Intravenous Use Only After…
FDA recall event 85916 · Class III · HF Acquisition Co. LLC
Key facts
| Event ID | 85916 |
|---|---|
| Recall numbers | D-1392-2020 |
| Recalling firm | HF Acquisition Co. LLC |
| Product type | Drugs |
| Products | 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 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state. |
| Initiation date | Jun 17, 2020 |
| Report date | Jul 29, 2020 |
| Termination date | Apr 13, 2021 |
| City | Mukilteo |
| State | WA |
| Country | United States |
| FEI number | 3014534 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: