Device recall
Z-1682-2012: Altrus Thermal Tissue Fusion, Tissue Fusion Handpiece 10 mm O.D., 23 cm Shaft…
FDA device recall · Class II · ConMed Electrosurgery
Key facts
| Recall number (Z-number) | Z-1682-2012 |
|---|---|
| Recall event | 61821 |
| Product | Altrus Thermal Tissue Fusion, Tissue Fusion Handpiece 10 mm O.D., 23 cm Shaft, Catalog Number 60-9511-001, Sterile/EO. 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 tissue bundles… |
| Product code | GEI |
| Recalling firm | ConMed Electrosurgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 5, 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