Device recall
Z-1198-2010: Pnemosure Insufflators, model numbers 620-040-600 and 620-040-610, manufactured…
FDA device recall · Class II · Stryker Endoscopy
Key facts
| Recall number (Z-number) | Z-1198-2010 |
|---|---|
| Recall event | 50777 |
| Product | Pnemosure Insufflators, model numbers 620-040-600 and 620-040-610, manufactured by Stryker Endoscopy, San Jose, CA. |
| Product code | HIF |
| Recalling firm | Stryker Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 24, 2011 |
| 510(k) numbers | K063367 |
| FEI number | 2936485 |
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