Device recall
Z-0292-2016: ECG Electrodes: 50007 Stablebase SBW55 50675 Stablebase SBW55-15 58051 Skintact…
FDA device recall · Class II · Leonhard Lang Medizintechnik GmbH
Key facts
| Recall number (Z-number) | Z-0292-2016 |
|---|---|
| Recall event | 72575 |
| Product | ECG Electrodes: 50007 Stablebase SBW55 50675 Stablebase SBW55-15 58051 Skintact W-60 50547 Stablebase SBT60 Only OUS: 50476 Skintact W-60HP E3 I 58046 Skintact T-60 I Patz K920 58688 Dahlhausen 1900000440 59629 Cardionetics CN-15-W60 58789 Lessa 99.832.02 58872 EF Medica FS 50 LG 50359Ultragel… |
| Product code | DRX |
| Recalling firm | Leonhard Lang Medizintechnik GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 21, 2017 |
| 510(k) numbers | K024247 |
| FEI number | 6736 |
At a glance
- 1–9 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