Device recall
Z-2282-2010: ABC PROBE REF 160655 5 mm Footswitching Probe, QTY: 1 STERILE CONMED CORPORATION…
FDA device recall · Class II · ConMed Electrosurgery
Key facts
| Recall number (Z-number) | Z-2282-2010 |
|---|---|
| Recall event | 52030 |
| Product | ABC PROBE REF 160655 5 mm Footswitching Probe, QTY: 1 STERILE CONMED CORPORATION 525 French Rd, Utica, NY 13501 ASSEMBLED IN MEXICO ABC PROBE REF 160655 5 mm Footswitching Probe, QTY: 10 STERILE CONMED CORPORATION 525 FRENCH RD UTICA, NY 13205 ASSEMBLED IN MEXICO Usage: Electrosurgical handpiece for… |
| Product code | GEI |
| Recalling firm | ConMed Electrosurgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 22, 2010 |
| 510(k) numbers | K925903 |
| FEI number | 3004491689 |
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