KODAK PROCESSOR *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1996-07-13 for KODAK PROCESSOR * manufactured by Eastman Kodak Co..

Event Text Entries

[16819800] Tanks are leaking at the overflow. Need to replace tanks.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number35495
MDR Report Key35495
Date Received1996-07-13
Date of Report1996-07-12
Date Added to Maude1996-08-20
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameKODAK PROCESSOR
Generic NamePROCESSOR
Product CodeIXW
Date Received1996-07-13
Model Number*
Catalog Number*
Lot Number*
ID Number117028
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Age*
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key36912
ManufacturerEASTMAN KODAK CO.
Manufacturer Address* ROCHESTER NY * US


Patients

Patient NumberTreatmentOutcomeDate
10 1996-07-13

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