MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2007-06-28 for MAGNA PURE SYSTEM 03670325001 manufactured by Roche Diagnostics.
[18493056]
User alleging sample contamination from the magna pure instrument causing downstream false positive cmv test results. If additional information is received, appropriate notification will be provided.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1823260-2007-05621 |
MDR Report Key | 1743610 |
Report Source | 05,06 |
Date Received | 2007-06-28 |
Date of Report | 2007-06-28 |
Date of Event | 2007-04-11 |
Date Facility Aware | 2007-05-29 |
Report Date | 2007-05-29 |
Date Mfgr Received | 2007-05-29 |
Date Added to Maude | 2010-07-08 |
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 | 0 |
Event Location | 3 |
Manufacturer Contact | SALLY BOWDEN |
Manufacturer Street | 9115 HAGUE RD. |
Manufacturer City | INDIANAPOLIS IN 46250 |
Manufacturer Country | US |
Manufacturer Postal | 46250 |
Manufacturer Phone | 3175214668 |
Manufacturer G1 | RD GMBH-PENZBERG |
Manufacturer Street | NONNENWALD 2. |
Manufacturer City | PENZBERG D68305 |
Manufacturer Postal Code | D68305 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MAGNA PURE SYSTEM |
Generic Name | NUCLEIC ACID PURIFICATION/AMPLIFICATION |
Product Code | OMI |
Date Received | 2007-06-28 |
Model Number | MAGNA PURE |
Catalog Number | 03670325001 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ROCHE DIAGNOSTICS |
Manufacturer Address | INDIANAPOLIS IN US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2007-06-28 |