Device recall
Z-1620-2008: FLAT DRAIN -10MM, CHARIKER-JETER DRESSING KITS (LARGE AND SMALL) -Product…
FDA device recall · Class III · Smith And Nephew, Inc. Wound Management Division
Key facts
| Recall number (Z-number) | Z-1620-2008 |
|---|---|
| Recall event | 47521 |
| Product | FLAT DRAIN -10MM, CHARIKER-JETER DRESSING KITS (LARGE AND SMALL) -Product numbers 6680217 and 6680221 - Wound Management Product. Indicated for patients who wold benefit from a suction device particularly as the device may promote wound healing. |
| Product code | BTA |
| Recalling firm | Smith And Nephew, Inc. Wound Management Division |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 18, 2008 |
| 510(k) numbers | K042134 |
| FEI number | 3006760724 |
At a glance
- 1–9 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