Drug recall
Ibuprofen-200 Advanced Pain Relief Tablets, (ibuprofen) 200mg, 24, 50 and 100 count bottles, Prepared by Reese…
FDA recall event 45488 · Class III · Reese Pharmaceutical Company
Key facts
| Event ID | 45488 |
|---|---|
| Recall numbers | D-052-2008 |
| Recalling firm | Reese Pharmaceutical Company |
| Product type | Drugs |
| Products | Ibuprofen-200 Advanced Pain Relief Tablets, (ibuprofen) 200mg, 24, 50 and 100 count bottles, Prepared by Reese Pharmaceutical Co., Cleveland, OH |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Impurity (6 month stabiility) |
| Initiation date | Oct 19, 2007 |
| Termination date | May 10, 2012 |
| City | Cleveland |
| State | OH |
| Country | United States |
| FEI number | 1518939 |
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