LS-202 Large LeadWear Combo Pack - Disposable ECG Monitoring component intended for use as a radiofrequency signal trans
FDA device recall Z-1660-2008 · posted 2008-09-16 · Terminated
Recall details
- Recalling firm
- Lifesync Corporation
- Reason for recall
- LifeSync Wireless ECG System - Intermittent failure when using LS-202 and LS-232 LeadWear in conjunction with LS-41245 and LS-41285 Adaptors. The out of box failure manifests as a V-Lead failure, 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
- Action taken
- Firm issued a Device Recall Letter on 12/14/2007. Users were requested to remove the product from inventory and discontinue use of the Large Sized LeadWear with the 12 Lead Adaptors. The current stock of product in inventory will be held under a stop shipment, pending destruction of non-conforming product.
- Root cause
- Nonconforming Material/Component
- Status
- Terminated
- Product code
- DRG
- Quantity affected
- 576 completed leadwire units
- Distribution
- Class II Recall - Nationwide Distribution.
- Date initiated
- 2007-12-13
- Date posted
- 2008-09-16
- Date terminated
- 2008-10-01
- Location
- Ft Lauderdale, FL
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| LIFESYNE SYSTEMS (K030795) | Gmp/Companies, Inc. | 2003-08-05 |