Device recall
Z-1942-2020: Insufflation tubing to be used with varies insufflator units. REF 031200-10; REF…
FDA device recall · Class III · Karl Storz Endoscopy
Key facts
| Recall number (Z-number) | Z-1942-2020 |
|---|---|
| Recall event | 85388 |
| Product | Insufflation tubing to be used with varies insufflator units. REF 031200-10; REF 031322-10; REF 031532-10; REF 031622-10 |
| Product code | NKC |
| Recalling firm | Karl Storz Endoscopy |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 28, 2022 |
| FEI number | 3007475226 |
At a glance
- None 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