Device recall
Z-2233-2009: SKINTACT Electrodes for Defibrillation, 10X REF DF20, Rx only, Manufactured by…
FDA device recall · Class II · Leonhard Lang Gmbh
Key facts
| Recall number (Z-number) | Z-2233-2009 |
|---|---|
| Recall event | 52794 |
| Product | SKINTACT Electrodes for Defibrillation, 10X REF DF20, Rx only, Manufactured by Leonhard Lang GmbH, Archenweg 56, 6020 Innsbruck, Austria. The device is non-sterile and single use. For use on adults and children over eight years old for external defibrillation, pacing, monitoring, and cardioversion. |
| Product code | MKJ |
| Recalling firm | Leonhard Lang Gmbh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 17, 2011 |
| 510(k) numbers | K072233 |
| FEI number | 6736 |
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