MAGNA PURE SYSTEM 03670325001

MAUDE Adverse Event Report

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.

Event Text Entries

[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


MAUDE Entry Details

Report Number1823260-2007-05621
MDR Report Key1743610
Report Source05,06
Date Received2007-06-28
Date of Report2007-06-28
Date of Event2007-04-11
Date Facility Aware2007-05-29
Report Date2007-05-29
Date Mfgr Received2007-05-29
Date Added to Maude2010-07-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location3
Manufacturer ContactSALLY BOWDEN
Manufacturer Street9115 HAGUE RD.
Manufacturer CityINDIANAPOLIS IN 46250
Manufacturer CountryUS
Manufacturer Postal46250
Manufacturer Phone3175214668
Manufacturer G1RD GMBH-PENZBERG
Manufacturer StreetNONNENWALD 2.
Manufacturer CityPENZBERG D68305
Manufacturer Postal CodeD68305
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMAGNA PURE SYSTEM
Generic NameNUCLEIC ACID PURIFICATION/AMPLIFICATION
Product CodeOMI
Date Received2007-06-28
Model NumberMAGNA PURE
Catalog Number03670325001
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerROCHE DIAGNOSTICS
Manufacturer AddressINDIANAPOLIS IN US


Patients

Patient NumberTreatmentOutcomeDate
10 2007-06-28

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