MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2020-03-31 for POWERHEART G5 KIT, AUTO, DAN/INTL ENG G5A-14A manufactured by Cardiac Science Corporation.
[186752165]
Zoll medical corporation has not received the device for evaluation and this complaint is still under investigation.
Patient Sequence No: 1, Text Type: N, H10
[186752166]
Complainant alleged that during functional testing,the device displayed an "ecg fault -501" error message. Complainant did not indicate that there was any patient involvement in the reported malfunction.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2112020-2020-00205 |
MDR Report Key | 9903663 |
Report Source | FOREIGN |
Date Received | 2020-03-31 |
Date of Report | 2020-03-10 |
Date Mfgr Received | 2020-03-10 |
Device Manufacturer Date | 2019-02-06 |
Date Added to Maude | 2020-03-31 |
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 | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Street | 269 MILL ROAD |
Manufacturer City | CHELMSFORD MA 01824 |
Manufacturer Country | US |
Manufacturer Postal | 01824 |
Manufacturer Phone | 9784219552 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | POWERHEART G5 KIT, AUTO, DAN/INTL ENG |
Generic Name | AUTOMATED EXTERNAL DEFIBRILLATOR |
Product Code | MKJ |
Date Received | 2020-03-31 |
Model Number | G5A-14A |
Catalog Number | G5A-14A |
Lot Number | NA |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CARDIAC SCIENCE CORPORATION |
Manufacturer Address | 500 BURDICK PARKWAY DEERFIELD WI 535319692 US 535319692 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-31 |