ALERE ISCREEN 9 PANEL TEST (DOA-194)

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2017-10-30 for ALERE ISCREEN 9 PANEL TEST (DOA-194) manufactured by Alere San Diego, Inc..

Event Text Entries

[91220248] Investigation pending.
Patient Sequence No: 1, Text Type: N, H10


[91220249] The customer reported receiving one false positive thc result and one false positive coc result on one patient using the alere iscreen 9 panel test. Confirmatory testing was conducted and produced negative results for both drugs. Although requested, no additional information was provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2027969-2017-00159
MDR Report Key6989010
Report SourceCONSUMER
Date Received2017-10-30
Date of Report2017-10-04
Date of Event2017-10-03
Date Mfgr Received2018-08-02
Date Added to Maude2017-10-30
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 ContactYA-LING KING
Manufacturer Street9975 SUMMERS RIDGE ROAD
Manufacturer CitySAN DIEGO CA 92121
Manufacturer CountryUS
Manufacturer Postal92121
Manufacturer Phone8588052084
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameALERE ISCREEN 9 PANEL TEST (DOA-194)
Generic NameENZYME IMMUNOASSAY, COCAINE AND COCAINE METABOLITES
Product CodeDIO
Date Received2017-10-30
Returned To Mfg2018-07-27
Model NumberDOA-194
Lot NumberDOA7020215
Device Expiration Date2019-01-31
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerALERE SAN DIEGO, INC.
Manufacturer Address9975 SUMMERS RIDGE ROAD SAN DIEGO CA 92121 US 92121


Patients

Patient NumberTreatmentOutcomeDate
10 2017-10-30

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