RESPIRATORY FORCE MEASURING 395946

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 2002-11-27 for RESPIRATORY FORCE MEASURING 395946 manufactured by Rusch Inc..

Event Text Entries

[285875] Customer reports the out-of box failure of device; does not work.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2429473-2002-00213
MDR Report Key431001
Report Source06
Date Received2002-11-27
Date of Report2002-11-21
Date Mfgr Received2002-11-04
Date Added to Maude2002-12-06
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 ContactNICOLE BLACKMAN
Manufacturer Street2450 MEADOWBROOK PARKWAY
Manufacturer CityDULUTH GA 30136
Manufacturer CountryUS
Manufacturer Postal30136
Manufacturer Phone7706230816
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRESPIRATORY FORCE MEASURING
Generic NameRESPIRATORY - OXYGEN DELIVERY
Product CodeBXR
Date Received2002-11-27
Model NumberNA
Catalog Number395946
Lot NumberUNK
ID NumberNA
OperatorOTHER
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key419984
ManufacturerRUSCH INC.
Manufacturer Address2450 MEADOWBROOK PARKWAY DULUTH GA 30096 US
Baseline Brand NameRESPIRATORY FORCE MEASURING
Baseline Model NoNA
Baseline Catalog No395946
Baseline IDNA
Baseline Shelf Life ContainedN
Baseline Shelf Life [Months]60
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
10 2002-11-27

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