GILSDORF GASTROSTOMY CATHETER E3430

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1999-05-19 for GILSDORF GASTROSTOMY CATHETER E3430 manufactured by Rusch, Inc..

Event Text Entries

[129059] It is alleged that the balloon inflation port plug popped out. The device had been in place for approx 1 month.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2429473-1999-00044
MDR Report Key224391
Report Source05
Date Received1999-05-19
Date of Report1999-05-18
Date of Event1999-05-17
Date Mfgr Received1999-05-17
Date Added to Maude1999-05-25
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
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGILSDORF GASTROSTOMY CATHETER
Generic NameGASTROSTOMY CATHETER
Product CodeKDH
Date Received1999-05-19
Model NumberNA
Catalog NumberE3430
Lot Number726030
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key217594
ManufacturerRUSCH, INC.
Manufacturer Address2450 MEADOWBROOK PKWY. DULUTH GA 30096 US
Baseline Brand NameGILSDORF GASTROSTOMY CATHETER
Baseline Generic NameGASTROSTOMY CATHETER
Baseline Model NoNA
Baseline Catalog NoE3430
Baseline IDNA
Baseline Device FamilyGASTROSTOMY CATHETER
Baseline Shelf Life Contained*
Baseline Shelf Life [Months]59
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK891371
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1999-05-19

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