GASTROSTOMY CATHETERS E3314

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 1998-11-10 for GASTROSTOMY CATHETERS E3314 manufactured by Rusch, Inc..

Event Text Entries

[144651] Leakage occurred around the tube insertion. The dr took off the tape, pulled the tube, and found that the balloon had burst.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2429473-1998-00071
MDR Report Key197205
Report Source05
Date Received1998-11-10
Date of Report1998-11-10
Date of Event1998-07-23
Date Mfgr Received1998-10-28
Date Added to Maude1998-11-18
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 NameGASTROSTOMY CATHETERS
Generic NameTRIPLE-PORT GASTROSTOMY CATHETERS
Product CodeKDH
Date Received1998-11-10
Model NumberNA
Catalog NumberE3314
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key191596
ManufacturerRUSCH, INC.
Manufacturer Address2450 MEADOWBROOK PKWY. DULUTH GA 30096 US
Baseline Brand NameTRIPLE-PORT GASTROSTOMY CATHETERS
Baseline Generic NameGASTROSTOMY CATHETER
Baseline Model NoNA
Baseline Catalog NoE3314
Baseline IDNA
Baseline Device FamilyGASTROSTOMY CATHETER
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK891371
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 1998-11-10

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.