Model Number 1011-0139-03 |
Device Problem
Energy Output Problem (1431)
|
Patient Problem
No Patient Involvement (2645)
|
Event Type
malfunction
|
Manufacturer Narrative
|
Zoll medical corporation has not received the device for evaluation and this complaint is still under investigation.
|
|
Event Description
|
Complainant alleged that during a routine shift check by a clinician, the associated defibrillator's defib output was out of specification using these internal handles.Complainant indicated that there was no patient involvement in the reported malfunction.
|
|
Manufacturer Narrative
|
The complainant was contacted for return of the device.The customer has responded and indicated the device will not be returning to zoll.
|
|
Search Alerts/Recalls
|