MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2015-01-07 for HEARTSTART MRX - EMS DEFIBRILLATOR M3536A manufactured by Philips Medical Systems.
[5305752]
It was reported to philips that the device would not acquire leads ecg and was showing a "device error. Service required" message with a red x and chip. There was no negative pt impact.
Patient Sequence No: 1, Text Type: D, B5
[12642797]
Pr#: (b)(4). A follow up report will be submitted upon completion of the investigation.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1218950-2015-00073 |
MDR Report Key | 4407204 |
Report Source | 06 |
Date Received | 2015-01-07 |
Date of Report | 2014-12-09 |
Date Mfgr Received | 2014-12-09 |
Device Manufacturer Date | 2011-06-01 |
Date Added to Maude | 2015-01-26 |
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 |
Reporter Occupation | PARAMEDIC |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | GREG THEOKAS |
Manufacturer Street | 3000 MINUTEMAN RD. |
Manufacturer City | ANDOVER MA 018101099 |
Manufacturer Country | US |
Manufacturer Postal | 018101099 |
Manufacturer Phone | 9786871501 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HEARTSTART MRX - EMS DEFIBRILLATOR |
Generic Name | DEFIBRILLATOR |
Product Code | MJK |
Date Received | 2015-01-07 |
Returned To Mfg | 2014-12-15 |
Model Number | M3536A |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PHILIPS MEDICAL SYSTEMS |
Manufacturer Address | 3000 MINUTEMAN RD. ANDOVER MA 01810109 US 01810 1099 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-01-07 |