Device recall
Z-1678-2012: Altrus Energy Source REF 60-9500-120 Tissue Fusion Energy Source ConMed…
FDA device recall · Class II · ConMed Electrosurgery
Key facts
| Recall number (Z-number) | Z-1678-2012 |
|---|---|
| Recall event | 61814 |
| Product | Altrus Energy Source REF 60-9500-120 Tissue Fusion Energy Source ConMed Corporation 525 French Rd, Utica, NY 13502, MDSS GmbH, Germany. The Altrus Thermal Tissue Fusion System is comprised of a dedicated energy source and disposable handpiece used to ligate (seal) and divide (cut) blood vessels and… |
| Product code | GEI |
| Recalling firm | ConMed Electrosurgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 19, 2012 |
| 510(k) numbers | K101534 |
| 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