ABBOTT COMMANDER PPC 3A46-01

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2000-11-01 for ABBOTT COMMANDER PPC 3A46-01 manufactured by Abbott Manufacturing, Inc..

Event Text Entries

[20992365] Commander fpc negative control was edited with negative control dispense volumes as 10ul. Date of editing was in 1998.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1628664-2000-00059
MDR Report Key303422
Report Source06
Date Received2000-11-01
Date of Report2000-10-31
Date of Event2000-10-02
Date Mfgr Received2000-10-02
Device Manufacturer Date1995-11-01
Date Added to Maude2000-11-08
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 Location0
Manufacturer ContactPAUL LANDESMAN
Manufacturer Street200 ABBOTT PARK RD
Manufacturer CityABBOTT PARK IL 600643500
Manufacturer CountryUS
Manufacturer Postal600643500
Manufacturer Phone8479372688
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameABBOTT COMMANDER PPC
Generic NameEIA FOR DETECTION OF HCV ANTIBODY
Product CodeLQI
Date Received2000-11-01
Model NumberNA
Catalog Number3A46-01
Lot NumberNA
ID NumberNA
OperatorUNKNOWN
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key293657
ManufacturerABBOTT MANUFACTURING, INC.
Manufacturer Address1921 HURD DR. IRVING TX 75038 US
Baseline Brand NameABBOTT COMMANDER FPC
Baseline Generic NameAUTOMATED SYSTEM FOR THE PROCESSING OF EIAS
Baseline Model NoNA
Baseline Catalog No3A46-01
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2000-11-01

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