Device recall
Z-1879-2019: Replacement ECG leadwires with snap ends REF/Catalog Number Description…
FDA device recall · Class III · GE Healthcare, LLC
Key facts
| Recall number (Z-number) | Z-1879-2019 |
|---|---|
| Recall event | 82937 |
| Product | Replacement ECG leadwires with snap ends REF/Catalog Number Description 2106386-101 Replacement ECG Leadwire, snap, LL, AHA, 130 cm/ 51 in The reusable ECG leadwire sets enable ECG monitoring with GE equipment requiring rectangular 11-pin ECG trunk cable. Use leadwire sets with ECG trunk cable or… |
| Product code | DSA |
| Recalling firm | GE Healthcare, LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 24, 2024 |
| FEI number | 2126677 |
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