Device recall
Z-0400-2010: Endoscopic Linear Cutter Reload, 45 mm Blue, product code PLCR45B; Endoscopic…
FDA device recall · Class II · Surgical Devices/Covidien
Key facts
| Recall number (Z-number) | Z-0400-2010 |
|---|---|
| Recall event | 53694 |
| Product | Endoscopic Linear Cutter Reload, 45 mm Blue, product code PLCR45B; Endoscopic Linear Cutter Reload, 45 mm Green, product code PLCR45G; Reusable Endoscopic Linear Cutter, 60 mm, product code PLC60; Endoscopic Linear Cutter Reload, 60 mm Blue, product code PLCR60B; Endoscopic Linear Cutter Reload, 60… |
| Product code | GDW |
| Recalling firm | Surgical Devices/Covidien |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 8, 2010 |
| FEI number | 1219930 |
At a glance
- None Linked 510(k)s
- 10–99 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