CHEMSTRIP 10 UA 418003

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 2002-05-06 for CHEMSTRIP 10 UA 418003 manufactured by Roche Diagnostics.

Event Text Entries

[229832] Pt brought to er. Urine sample ran on suspect device. Result of negative leukocytes. Ran visually and negative leukocytes. Performed microscopic examination and 40-50 granulocytes. Pt expired. Toxic levels of acetaminophen found in blood. Pt also tested positive for opiates.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1823260-2002-00133
MDR Report Key392686
Report Source05
Date Received2002-05-06
Date of Report2002-04-24
Date of Event2002-04-24
Date Mfgr Received2002-04-24
Date Added to Maude2002-05-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactDEBARA REEK
Manufacturer Street9115 HAGUE RD.
Manufacturer CityINDIANAPOLIS IN 46250
Manufacturer CountryUS
Manufacturer Postal46250
Manufacturer Phone3175763857
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCHEMSTRIP 10 UA
Generic NameURINALYSIS TEST STRIP
Product CodeJRE
Date Received2002-05-06
Model NumberNA
Catalog Number418003
Lot Number28830241
ID NumberNA
Device Expiration Date2002-06-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeNA
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key381715
ManufacturerROCHE DIAGNOSTICS
Manufacturer AddressSANHOFER STRASSE 116 MANNHEIM * D-68298
Baseline Brand NameCHEMSTRIP 10 UA
Baseline Generic NameCHEMSTRIP 10
Baseline Model NoNA
Baseline Catalog No418003
Baseline IDNA
Baseline Device FamilyURINALYSIS TEST STRIPS
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]21
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK896454
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Death 2002-05-06

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