| Model Number |
E SERIES |
| Medical Device Problem Code |
Failure of Device to Self-Test (2937)
|
| Health Effect - Clinical Code |
No Patient Involvement (2645)
|
|
Type of Reportable Event
|
Malfunction
|
|
Additional Manufacturer Narrative
|
|
The malfunction was duplicated and the biphasic flex cable was replaced to resolve the malfunction.The device was recertified and returned to the customer.Analysis of reports of this type has not identified an increase in trend.
|
| |
|
Event or Problem Description
|
|
Complainant alleged that during a routine shift check by a clinician, the device failed self test.Complainant indicated that there was no patient involvement in the reported malfunction.
|
| |
|
Search Alerts/Recalls
|