MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2012-03-23 for CARDIOCAP 5 manufactured by Ge Healthcare.
[2575373]
It was reported that the cardiocap 5 monitor was not syncing correctly with the lithotripsy unit. There was no serious injury or death associated with this event, nor was medical intervention required. Ge healthcare's investigation is ongoing. A f/u report will be submitted once the investigation has been completed.
Patient Sequence No: 1, Text Type: D, B5
[9840177]
The device manufacture date is unk.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 9610105-2012-00016 |
MDR Report Key | 2507780 |
Report Source | 06 |
Date Received | 2012-03-23 |
Date of Report | 2012-02-23 |
Date of Event | 2012-02-23 |
Date Mfgr Received | 2012-02-23 |
Date Added to Maude | 2012-09-04 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 0 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | JOY SONSALLA |
Manufacturer Street | 3000 W. GRANDVIEW BLVD. W450 |
Manufacturer City | WAUKEESHA WI 53188 |
Manufacturer Country | US |
Manufacturer Postal | 53188 |
Manufacturer Phone | 2625482661 |
Manufacturer G1 | GE HEALTHCARE |
Manufacturer City | HELSINKI |
Manufacturer Country | FI |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CARDIOCAP 5 |
Generic Name | PATIENT MONITOR |
Product Code | MLD |
Date Received | 2012-03-23 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | GE HEALTHCARE |
Manufacturer Address | HELSINKI FI |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2012-03-23 |