Device recall
Z-2561-2021: Covidien HysteroLux Fluid Management System Control Unit, REF: 72205000
FDA device recall · Class II · WOM World of Medicine AG
Key facts
| Recall number (Z-number) | Z-2561-2021 |
|---|---|
| Recall event | 88426 |
| Product | Covidien HysteroLux Fluid Management System Control Unit, REF: 72205000 |
| Product code | HIG |
| Recalling firm | WOM World of Medicine AG |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K173489 |
| FEI number | 3001556604 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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