MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-07-15 for HEARTSTART FR3 989803149941 manufactured by Philips Medical Systems.
[50387023]
Patient Sequence No: 1, Text Type: N, H10
[50387024]
It has been reported that the qcpr meter is not functioning properly.
Patient Sequence No: 1, Text Type: D, B5
[58854953]
(b)(4). Qcpr meter not manufactured by philips.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 3030677-2016-01648 |
MDR Report Key | 5798321 |
Date Received | 2016-07-15 |
Date of Report | 2016-07-12 |
Date Mfgr Received | 2016-07-12 |
Device Manufacturer Date | 2014-07-01 |
Date Added to Maude | 2016-07-15 |
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 Contact | MRS. DANA TACKETT |
Manufacturer Street | 22100 BOTHELL EVERETT HWY |
Manufacturer City | BOTHELL WA 980218431 |
Manufacturer Country | US |
Manufacturer Postal | 980218431 |
Manufacturer Phone | 8887445477 |
Manufacturer G1 | PHILIPS HEALTHCARE - BOTHELL |
Manufacturer Street | 22100 BOTHELL-EVERETT HWY BLDG A |
Manufacturer City | BOTHELL WA 98021 |
Manufacturer Country | US |
Manufacturer Postal Code | 98021 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HEARTSTART FR3 |
Generic Name | CPR METER |
Product Code | LIX |
Date Received | 2016-07-15 |
Model Number | 989803149941 |
ID Number | N/A |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PHILIPS MEDICAL SYSTEMS |
Manufacturer Address | 22100 BOTHELL EVERETT HWY BOTHELL WA 980218431 US 980218431 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2016-07-15 |