Device recall
Z-0316-2007: Posterior Acetabular Retractor-Left with Light Cord Bracket, Model…
FDA device recall · Class II · Whiteside Biomechanics
Key facts
| Recall number (Z-number) | Z-0316-2007 |
|---|---|
| Recall event | 36760 |
| Product | Posterior Acetabular Retractor-Left with Light Cord Bracket, Model #BIO-1-1050-A, and Posterior Acetabular Retractor-Right with Light Cord Bracket, Model #BIO-1-1051-A, packaged 1 retractor (left or right retractor) per plastic bag. The firm name on the label is Whiteside Biomechanics, Inc., St… |
| Product code | GAD |
| Recalling firm | Whiteside Biomechanics |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 11, 2008 |
| FEI number | 3002477077 |
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