Device recall
Z-1877-2019: Replacement leadwires with grabber ends: REF/Catalog Number Description…
FDA device recall · Class III · GE Healthcare, LLC
Key facts
| Recall number (Z-number) | Z-1877-2019 |
|---|---|
| Recall event | 82937 |
| Product | Replacement leadwires with grabber ends: REF/Catalog Number Description 2106388-005 Replacement ECG Leadwire, grabber, BRN V, AHA, 74 cm/ 29 in 2106388-101 Replacement ECG Leadwire, grabber, LL , AHA, 130 cm/ 51 in 2106388-103 Replacement ECG Leadwire, grabber, GRN RL, AHA, 130 cm/ 2106388-107… |
| 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