RUSCH 120100-000070

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,06 report with the FDA on 2003-11-04 for RUSCH 120100-000070 manufactured by Willy Rusch Gmbh.

Event Text Entries

[317849] The customer reports that the balloon leaked whilst the instrument was in use.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610520-2003-00244
MDR Report Key494769
Report Source01,06
Date Received2003-11-04
Date of Report2003-10-29
Date Mfgr Received2003-10-01
Date Added to Maude2003-11-13
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactWILLIAM SLEVIN, MANAGER
Manufacturer Street2450 MEADOWBROOK PARKWAY
Manufacturer CityDULUTH GA 30096
Manufacturer CountryUS
Manufacturer Postal30096
Manufacturer Phone7706230816
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRUSCH
Generic NameSENGSTAKEN TUBE
Product CodeKDH
Date Received2003-11-04
Returned To Mfg2003-01-10
Model NumberNA
Catalog Number120100-000070
Lot Number01391
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key483484
ManufacturerWILLY RUSCH GMBH
Manufacturer AddressWILLY-RUSCH STRASSE 4-10 KERNEN I.R. GM 71394
Baseline Brand NameRUSCH
Baseline Generic NameTRACHEOFLEX TRACHEAL TUBE SHORT
Baseline Model NoNA
Baseline Catalog No120100-000070
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2003-11-04

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