Device recall
Z-1660-2008: LS-202 Large LeadWear Combo Pack - Disposable ECG Monitoring component intended…
FDA device recall · Class II · Lifesync Corporation
Key facts
| Recall number (Z-number) | Z-1660-2008 |
|---|---|
| Recall event | 47336 |
| Product | LS-202 Large LeadWear Combo Pack - Disposable ECG Monitoring component intended for use as a radiofrequency signal transmitter and receiver of electrocardiograph physiological signals which are displayed on the ECG monitors of various manufacturers' systems that have been validated for… |
| Product code | DRG |
| Recalling firm | Lifesync Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 1, 2008 |
| 510(k) numbers | K030795 |
| FEI number | 1000403400 |
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