Device recall
Z-0751-2017: Rochester-Pean Hemostatic Forceps 61/4, Curved, Sterile. The Rochester-Pean…
FDA device recall · Class II · Integra York PA, Inc
Key facts
| Recall number (Z-number) | Z-0751-2017 |
|---|---|
| Recall event | 75710 |
| Product | Rochester-Pean Hemostatic Forceps 61/4, Curved, Sterile. The Rochester-Pean Hemostatic Forceps 61/4 Curved are single-use sterile surgical instruments intended for cutting and grasping tissue in general surgical procedures. |
| Product code | GEN |
| Recalling firm | Integra York PA, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 2017 |
| FEI number | 2518040 |
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