Drug recall
Endocet (oxycodone and acetaminophen tablets, USP), 10/325 mg, C-II, 100-count bottles, Rx Only, Manufactured…
FDA recall event 59140 · Class I · Endo Pharmaceuticals, Inc.
Key facts
| Event ID | 59140 |
|---|---|
| Recall numbers | D-908-2011 |
| Recalling firm | Endo Pharmaceuticals, Inc. |
| Product type | Drugs |
| Products | Endocet (oxycodone and acetaminophen tablets, USP), 10/325 mg, C-II, 100-count bottles, Rx Only, Manufactured for Endo Pharmaceuticals Inc., Chadds Ford, PA, 19317, By: Novartis, Lincoln, NE, 68501… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Adulterated presence of foreign tablets: Bottles of Endocet 10/325-mg tablets, (100-count bottles) may contain some Endocet 10/650-mg tablets. |
| Initiation date | Jun 24, 2011 |
| Termination date | Sep 5, 2013 |
| City | Chadds Ford |
| State | PA |
| Country | United States |
| FEI number | 3001578003 |
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