Device recall
Z-1997-2014: Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-1997-2014 |
|---|---|
| Recall event | 68243 |
| Product | Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 31151090 Product Usage: The device is intended to provide padding under the patient, and help maintain the position of an anesthetized patient during surgery. |
| Product code | CCX |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 4, 2015 |
| FEI number | 1282497 |
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