Device recall
Z-0409-2010: Intelligent Battery Pack, product code iB100; Intelligent Battery Charger and…
FDA device recall · Class II · Surgical Devices/Covidien
Key facts
| Recall number (Z-number) | Z-0409-2010 |
|---|---|
| Recall event | 53694 |
| Product | Intelligent Battery Pack, product code iB100; Intelligent Battery Charger and Power Supply, product code iB1C1; Intelligent Battery Insertion Guide, product code iBIG-1; Intelligent Battery Insertion Tool, product code iBIT-1. |
| Product code | GDW |
| Recalling firm | Surgical Devices/Covidien |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 8, 2010 |
| 510(k) numbers | K091215 |
| FEI number | 1219930 |
At a glance
- 1–9 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