Drug recall
Diazepam Oral Solution (Concentrate), 25 mg per 5 mL (5 mg/mL), 30 mL BOTTLE and DROPPER, Rx Only, Distributed…
FDA recall event 89551 · Class II · Lannett Company, Inc.
Key facts
| Event ID | 89551 |
|---|---|
| Recall numbers | D-0558-2022 |
| Recalling firm | Lannett Company, Inc. |
| Product type | Drugs |
| Products | Diazepam Oral Solution (Concentrate), 25 mg per 5 mL (5 mg/mL), 30 mL BOTTLE and DROPPER, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1768-36. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Failed Impurities/Degradation Specifications: Out of specification results for related substances. |
| Initiation date | Feb 9, 2022 |
| Report date | Feb 23, 2022 |
| Termination date | May 1, 2023 |
| City | Philadelphia |
| State | PA |
| Country | United States |
| FEI number | 2510865 |
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: