Device recall
Z-0145-2014: Individual units labeled in part: REF: 4630022; for S(a)line resectoscopes…
FDA device recall · Class II · Richard Wolf Medical Instruments Corp.
Key facts
| Recall number (Z-number) | Z-0145-2014 |
|---|---|
| Recall event | 66457 |
| Product | Individual units labeled in part: REF: 4630022; for S(a)line resectoscopes; Vaporization electrode, sterite; 4mm telescope 30 25 / 12: only for continuous irrigation sheath 24,5 Fr.; LOT 426111; 2011/06; 2016/06; STERILE; RICHARD WOLF; Cartons of 3 units labeled in part: REF 46300223; Vaporization… |
| Product code | FJL |
| Recalling firm | Richard Wolf Medical Instruments Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 24, 2017 |
| 510(k) numbers | K062720 |
| FEI number | 1418479 |
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