Zoll M Series Automated Defibrillator (AED)
This recall has been terminated (originally issued September 17, 2004).
- Company
- Zoll Medical Corporation
- Recall Initiated
- August 2, 2004
- Posted
- September 17, 2004
- Terminated
- February 13, 2017
- Recall Number
- Z-1472-04
- Quantity
- 5649 units
- Firm Location
- Chelmsford, MA
- Official Source
- View on FDA website ↗
Reason for Recall
Visual Sreen display and audible prompt may not advise to 'Press Shock'
Distribution
Nationwide
Lot / Code Info
Software Versions below 34.00
Root Cause
Other
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.
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