MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-11-24 for GAMBRO manufactured by Gambro Americas Headquarters.
[20746330]
D2 flowmeter failure 301 and flow balance error d1-d2 144.
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5018374 |
MDR Report Key | 1916798 |
Date Received | 2010-11-24 |
Date of Report | 2010-11-24 |
Date of Event | 2010-04-23 |
Date Added to Maude | 2010-12-09 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Reporter Occupation | RISK MANAGER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | GAMBRO |
Generic Name | PHOENIX DIALYSIS MACHINE |
Product Code | FII |
Date Received | 2010-11-24 |
Lot Number | GE35806352 |
ID Number | PH5789 |
Device Availability | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | GAMBRO AMERICAS HEADQUARTERS |
Manufacturer Address | 14143 DENVER WEST PKWY LAKEWOOD CO 80401 US 80401 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2010-11-24 |