COBAS TAQSCREEN MPX TEST 04584252190

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2013-11-22 for COBAS TAQSCREEN MPX TEST 04584252190 manufactured by Roche Molecular Systems.

Event Text Entries

[17614035] A blood center in the us filed a complaint alleging that a (b)(6) sample that was (b)(6) generated a (b)(6) result in pools of 6 testing on (b)(6) 2013 with the cobas taqscreen mpx test. The donor unit was not released due to the positive serology results. The donor sample has been requested for investigative testing.
Patient Sequence No: 1, Text Type: D, B5


[17755456] A definitive conclusion cannot be drawn at this time, as the investigation into this issue is ongoing. The outcome of the investigation will be communicated through a follow-up report. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2243471-2013-00034
MDR Report Key3484161
Report Source05
Date Received2013-11-22
Date of Report2013-11-01
Date of Event2013-10-30
Date Mfgr Received2013-11-01
Date Added to Maude2014-03-04
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 Location0
Manufacturer ContactVINCENT STAGNITTO
Manufacturer Street1080 US HWY 202S
Manufacturer CityBRANCHBURG NJ 088763733
Manufacturer CountryUS
Manufacturer Postal088763733
Manufacturer Phone9082537569
Single Use0
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOBAS TAQSCREEN MPX TEST
Generic NameHEPATITIS VIRAL B DNA DETECTION
Product CodeMKT
Date Received2013-11-22
Catalog Number04584252190
Lot NumberS00265
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerROCHE MOLECULAR SYSTEMS
Manufacturer Address1080 US HW 202S BRANCHBURG NJ 08876373 US 08876 3733


Patients

Patient NumberTreatmentOutcomeDate
10 2013-11-22

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.