MULTI-DRUG 5 PANEL SCREEN TEST DOA-654

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,health professional, report with the FDA on 2017-08-25 for MULTI-DRUG 5 PANEL SCREEN TEST DOA-654 manufactured by Alere San Diego, Inc..

Event Text Entries

[83749177] Investigation conclusion: the customer's observation was not replicated in-house with retention products. Retention devices were tested with in-house drug free donor urine and all devices showed expected negative results for all analytes at read time. No false positive results were observed during in-house testing. Manufacturing batch record review did not uncover any abnormalities. Based on the information available, there is no indication of a product deficiency and no corrective action is required.
Patient Sequence No: 1, Text Type: N, H10


[83749178] The customer reported 40 occurrences of false positive results on all drugs using the multi-drug 5 panel screen on random donors starting in (b)(6) of 2017. Testing at an external laboratory provided negative results. The customer reported that out of 325 devices used, 40 produced false positive results.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2027969-2017-00136
MDR Report Key6822697
Report SourceCONSUMER,HEALTH PROFESSIONAL,
Date Received2017-08-25
Date of Report2017-08-08
Date Mfgr Received2017-08-08
Date Added to Maude2017-08-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
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 NameMULTI-DRUG 5 PANEL SCREEN TEST
Generic NameENZYME IMMUNOASSAY, COCAINE AND COCAINE METABOLITES
Product CodeDIO
Date Received2017-08-25
Model NumberDOA-654
Lot NumberDOA6090505
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
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 2017-08-25

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