COBAS TAQSCREEN MPX TEST V2.0 US-IVD 05969484190

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-05-12 for COBAS TAQSCREEN MPX TEST V2.0 US-IVD 05969484190 manufactured by Roche Molecular Systems.

Event Text Entries

[75381851] The investigation into this issue is currently on-going. The outcome of this investigation will be communicated through a follow-up report. The udi for the cobas taqscreen mpx test, v2. 0 us-ivd is: 00875197004045. The product common name was truncated and the complete name is "(b)(6)". (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[75381852] The customer alleged an increased frequency of unexpected reactivity in donor sample results using the cobas taqscreen mpx test, v2. 0 us-ivd, starting the (b)(6) 2017. The customer alleged this event has led to multiple donation losses, including blood, organ and cadaveric tissue donations. The customer reported the event to the fda. Four kit lots were involved in the customer allegation. This mdr is for kit lot x07609.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2243471-2017-00013
MDR Report Key6563574
Date Received2017-05-12
Date of Report2018-01-26
Date of Event2017-04-01
Date Mfgr Received2017-04-14
Date Added to Maude2017-05-12
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 FDA3
Event Location3
Manufacturer ContactNA STACIE-ANN CREIGHTON
Manufacturer Street1080 US HWY 202 S NA
Manufacturer CityBRANCHBURG NJ 08876
Manufacturer CountryUS
Manufacturer Postal08876
Manufacturer Phone9082537112
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report0

Device Details

Brand NameCOBAS TAQSCREEN MPX TEST V2.0 US-IVD
Generic NameHUMAN IMMUNODEFICIENCY VIRUS TYPE 1 (HIV-1) GROUP M AND O RNA, HIV-2 RNA, HCV
Product CodeMTL
Date Received2017-05-12
Model NumberNA
Catalog Number05969484190
Lot NumberX07609
ID NumberNA
Device Expiration Date2018-04-30
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerROCHE MOLECULAR SYSTEMS
Manufacturer Address1080 US HWY 202 S NA 1080 US HWY 202 S NJ 08876 US 08876


Patients

Patient NumberTreatmentOutcomeDate
10 2017-05-12

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