Device recall
Z-2243-2024: WOM Tube Set for lrrlgatlon, single-use- Intended to transport irrigation fluid…
FDA device recall · Class II · WOM World Of Medicine AG
Key facts
| Recall number (Z-number) | Z-2243-2024 |
|---|---|
| Recall event | 94749 |
| Product | WOM Tube Set for lrrlgatlon, single-use- Intended to transport irrigation fluid to the patient in endoscopic surgeries. Distr. by Endoscopy Smith & Nephew Inc. REF Numbers: T0449-01 |
| Product code | HRX |
| Recalling firm | WOM World Of Medicine AG |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K062380 |
| FEI number | 3002914049 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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