Drug recall
Sepp, Compound Benzoin Tincture Packaged and Tincture 3,000 Bulk. Product Usage: Preoperative skin product
FDA recall event 64585 · Class III · CareFusion 213, LLC
Key facts
| Event ID | 64585 |
|---|---|
| Recall numbers | Z-1001-2013 |
| Recalling firm | CareFusion 213, LLC |
| Product type | Devices |
| Products | Sepp, Compound Benzoin Tincture Packaged and Tincture 3,000 Bulk. Product Usage: Preoperative skin product |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | An internal review of CareFusion's labeling for preoperative skin prep product codes was recently conducted. The labeling of the product codes identified above state that the contents of the package… |
| Initiation date | Mar 4, 2013 |
| Report date | Apr 3, 2013 |
| Termination date | May 12, 2014 |
| City | El Paso |
| State | TX |
| Country | United States |
| FEI number | 3004932373 |
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: