Device recall
Z-1001-2013: Sepp, Compound Benzoin Tincture Packaged and Tincture 3,000 Bulk. Product Usage…
FDA device recall · Class III · CareFusion 213, LLC
Key facts
| Recall number (Z-number) | Z-1001-2013 |
|---|---|
| Recall event | 64585 |
| Product | Sepp, Compound Benzoin Tincture Packaged and Tincture 3,000 Bulk. Product Usage: Preoperative skin product |
| Product code | OJU |
| Recalling firm | CareFusion 213, LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 12, 2014 |
| FEI number | 3004932373 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database