Device recall
Z-0701-2007: SCANLAN International Mobin-Uddin Vein Holder, Sterile, Disposable, single-use…
FDA device recall · Class II · Scanlan International Inc
Key facts
| Recall number (Z-number) | Z-0701-2007 |
|---|---|
| Recall event | 37596 |
| Product | SCANLAN International Mobin-Uddin Vein Holder, Sterile, Disposable, single-use, catalog #1001-761, Lot AZ115806. |
| Product code | KDC |
| Recalling firm | Scanlan International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 27, 2007 |
| FEI number | 2126670 |
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