Device recall
Z-1785-2013: Eon and Eon Mini charging system, model numbers Eon -3701 (Wall Charger), 3711…
FDA device recall · Class II · St. Jude Medical
Key facts
| Recall number (Z-number) | Z-1785-2013 |
|---|---|
| Recall event | 63947 |
| Product | Eon and Eon Mini charging system, model numbers Eon -3701 (Wall Charger), 3711 (Portable Charger) and Eon Mini -3721 (Charger); This is a continuation of the firm's July 2012 recall. Product Usage: The Eon Wall Charger (3701) provides the capability to recharge the IPG Battery. The charger transmits… |
| Product code | LGW |
| Recalling firm | St. Jude Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 4, 2015 |
| PMA numbers | P010032, P010032S028 |
| FEI number | 1627487 |
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