Device recall
Z-0212-2007: Lone Star Medical Products, Inc. 1100 Series Aluminum Retractor Rings, Model…
FDA device recall · Class II · Lone Star Medical Products, Inc
Key facts
| Recall number (Z-number) | Z-0212-2007 |
|---|---|
| Recall event | 36592 |
| Product | Lone Star Medical Products, Inc. 1100 Series Aluminum Retractor Rings, Model #1104; manufactured by Lone Star Medical Products, Inc. |
| Product code | GAD |
| Recalling firm | Lone Star Medical Products, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 22, 2006 |
| FEI number | 1627186 |
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