Device recall
Z-3109-2017: Skintact Electrode for Defibrillation, Pacing, Monitoring, Cardioversion…
FDA device recall · Class I · Leonhard Lang Medizintechnik GmbH
Key facts
| Recall number (Z-number) | Z-3109-2017 |
|---|---|
| Recall event | 77949 |
| Product | Skintact Electrode for Defibrillation, Pacing, Monitoring, Cardioversion. Product Usage: Multifunction electrode for external defibrillation, pacing, cardioversion, and monitoring. The device is non-sterile and for single use only. Used with automated external defibrillators |
| Product code | MKJ |
| Recalling firm | Leonhard Lang Medizintechnik GmbH |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 9, 2020 |
| 510(k) numbers | K142803 |
| 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