Device recall
Z-0872-2007: Well Leg Holder With Boot, part of the Supine Universal Hip Distractor System…
FDA device recall · Class III · Smith & Nephew, Inc Endoscopy Division
Key facts
| Recall number (Z-number) | Z-0872-2007 |
|---|---|
| Recall event | 37792 |
| Product | Well Leg Holder With Boot, part of the Supine Universal Hip Distractor System; Ref (Part) #72200632; Manufactured for Smith & Nephew, Inc., Endoscopy Divsion, Andover, MA 01810. |
| Product code | NBH |
| Recalling firm | Smith & Nephew, Inc Endoscopy Division |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 16, 2008 |
| FEI number | 1643264 |
At a glance
- None 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