AXSYM DRUGS OF ABUSE TOXICOLOGY ASSAY DISK 3D54-08

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04,05 report with the FDA on 2008-02-05 for AXSYM DRUGS OF ABUSE TOXICOLOGY ASSAY DISK 3D54-08 manufactured by Abbott Laboratories.

Event Text Entries

[21955470] The customer stated a vrtx error occurred two times on the axsym analyzer while running pt samples. The customer had upgraded to axsym system software version 6. 1 the week prior in an effort to resolve the vrtx error. Drugs of abuse (doa)/ toxicology assay disk version 8. 0 was in use. The customer had edited the cutoff for amphetamines after installation of the doa disk. The customer was instructed to cycle power and reset the processing unit, and reminded to cycle power regularly. The issue was resolved. No impact to pt management was reported.
Patient Sequence No: 1, Text Type: D, B5


[22260994] This is an initial report. An investigation is in progress. A final report will be submitted when the investigation is complete.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1415939-2008-00019
MDR Report Key991055
Report Source04,05
Date Received2008-02-05
Date of Report2008-01-15
Date of Event2007-12-27
Date Mfgr Received2008-01-15
Date Added to Maude2008-09-29
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 ContactSUDARSHAN HEBBAR, MD, D-3MQC, AP6B
Manufacturer Street100 ABBOTT PARK RD.
Manufacturer CityABBOTT PARK IL 600646112
Manufacturer CountryUS
Manufacturer Postal600646112
Manufacturer Phone8479379677
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction Number1415939-2/01/08-001-C
Event Type3
Type of Report3

Device Details

Brand NameAXSYM DRUGS OF ABUSE TOXICOLOGY ASSAY DISK
Generic NameAMPHETAMINE TEST SYSTEM
Product CodeDKZ
Date Received2008-02-05
Model NumberNA
Catalog Number3D54-08
Lot NumberNA
ID NumberV 8.0
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeNA
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedB
Device Sequence No1
Device Event Key994069
ManufacturerABBOTT LABORATORIES
Manufacturer Address100 ABBOTT PARK RD. ABBOTT PARK IL 600643500 US


Patients

Patient NumberTreatmentOutcomeDate
10 2008-02-05

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