AUTOREADER II 7003009 936000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2002-11-05 for AUTOREADER II 7003009 936000 manufactured by Ortho-clinical Diagnostics.

Event Text Entries

[21396578] Customer reported that autoreader ii was showing increased amounts of negative optical density values on hbsag plates. No death or serious injury was associated with this incident. Note: during an audit of the complaint system, this complaint was determined to be a reportable event. This form is past the required 30 day reporting period.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2250051-2002-00665
MDR Report Key426864
Date Received2002-11-05
Date of Report2002-10-18
Date of Event2002-07-17
Date Facility Aware2002-07-26
Report Date2002-10-18
Date Reported to Mfgr2002-07-26
Date Added to Maude2002-11-13
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
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
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameAUTOREADER II
Generic NamePLATE READER
Product CodeLRH
Date Received2002-11-05
Model Number7003009
Catalog Number936000
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age9 YR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key415884
ManufacturerORTHO-CLINICAL DIAGNOSTICS
Manufacturer Address1001 US HWY 202 RARITAN NJ 088690606 US
Baseline Brand NameORTHO SUMMIT SAMPLE HANDLER
Baseline Generic NameSAMPLE HANDLER
Baseline Model No7003009
Baseline Catalog No936400
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2002-11-05

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