Device recall
Z-1150-2007: Bayonet Electrosurgical Pencil. P/N 9560575. The product is shipped in cases…
FDA device recall · Class II · Zinnanti Surgical Design LLC
Key facts
| Recall number (Z-number) | Z-1150-2007 |
|---|---|
| Recall event | 38458 |
| Product | Bayonet Electrosurgical Pencil. P/N 9560575. The product is shipped in cases containing 100 blades/pencils. |
| Product code | GEI |
| Recalling firm | Zinnanti Surgical Design LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 7, 2008 |
| 510(k) numbers | K930511 |
| FEI number | 1000135710 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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