ALERE TOX SCREEN DRUG CUP 4027750131

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 2014-05-30 for ALERE TOX SCREEN DRUG CUP 4027750131 manufactured by Alere San Diego, Inc..

Event Text Entries

[4606515] Caller alleging a false positive for all drugs including cocaine (coc). Caller stated a test would be run on one cup and get one result; then the specimen in a different cup would get a different result.
Patient Sequence No: 1, Text Type: D, B5


[12150961] Customer's observation was not replicated in-house with retention strips. Retention strip were tested 29 drug-free donor urine; all met/thc/opi/ppx/bar/coc/oxy/bzo/mdma results were negative. No false results were obtained. Manufacturing batch record review did not uncover any abnormalities. Root cause could not be determined from the information provided. Based on the information available, there is no indication of a product deficiency. This issue will be subject to tracking and trending. As there was no indication of a product deficiency, corrective action is not required at this time.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2027969-2014-00517
MDR Report Key3963493
Report Source05
Date Received2014-05-30
Date of Report2014-05-12
Date of Event2014-05-12
Date Mfgr Received2014-05-12
Date Added to Maude2014-08-04
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 ContactYA-LING KING
Manufacturer Street9975 SUMMERS RIDGE RD
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 TOX SCREEN DRUG CUP
Generic NameDRUGS OF ABUSE
Product CodeDKZ
Date Received2014-05-30
Model Number4027750131
Lot NumberDOA3090335
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALERE SAN DIEGO, INC.
Manufacturer AddressSAN DIEGO CA US


Patients

Patient NumberTreatmentOutcomeDate
10 2014-05-30

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