Zoll M Series Automated Defibrillator (AED)
FDA device recall Z-1472-04 · posted 2004-09-17 · Terminated
Recall details
- Recalling firm
- Zoll Medical Corporation
- Reason for recall
- Visual Sreen display and audible prompt may not advise to 'Press Shock'
- Action taken
- Zoll Medical notified consignees by letter on 8/2/04 via Certified Mail. Users are advised of the problem and the softtware upgrade.
- Root cause
- Other
- Status
- Terminated
- Product code
- MKT
- Quantity affected
- 5649 units
- Distribution
- Nationwide
- Date initiated
- 2004-08-02
- Date posted
- 2004-09-17
- Date terminated
- 2017-02-13
- Location
- Chelmsford, MA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| ZOLL M SERIES (K010257) | Zoll Medical Corp | 2001-02-28 |