| Model Number |
ACT2020 |
| Medical Device Problem Codes |
Device Alarm System (1012); Temperature Problem (3022)
|
| Health Effect - Clinical Code |
No Consequences Or Impact To Patient (2199)
|
| Date of Event |
02/18/2019
|
|
Type of Reportable Event
|
Malfunction
|
|
Additional Manufacturer Narrative
|
|
If information is provided in the future, a supplemental report will be issued.
|
| |
|
Event or Problem Description
|
|
According to the reporter, during ablation, the device had an alarm of high impedance.Replaced with another similar device and it worked fine which completed the procedure.There was no patient injury.
|
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|
Search Alerts/Recalls
|