Drug recall
Oxycodone Hydrochloride Oral Solution, USP 5 mg/5mL unit dose cups, Rx Only, Genus Lifesciences Inc. NDC…
FDA recall event 87044 · Class III · Genus Lifesciences Inc.
Key facts
| Event ID | 87044 |
|---|---|
| Recall numbers | D-0231-2021 |
| Recalling firm | Genus Lifesciences Inc. |
| Product type | Drugs |
| Products | Oxycodone Hydrochloride Oral Solution, USP 5 mg/5mL unit dose cups, Rx Only, Genus Lifesciences Inc. NDC 64950-354-05 Case NDC: 64950-354-450(40 unit dose cups) Case NDC 64950-354-55 (50 unit dose… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Presence of Foreign Substance: Particulate matter was found in multiple lots of product. |
| Initiation date | Dec 23, 2020 |
| Report date | Jan 20, 2021 |
| Termination date | Nov 5, 2021 |
| City | Allentown |
| State | PA |
| Country | United States |
| FEI number | 3003851100 |
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: