CONVATEC LOOP OSTOMY ROD * 22355

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 2005-05-02 for CONVATEC LOOP OSTOMY ROD * 22355 manufactured by Convatec,.

Event Text Entries

[15214825] Patient underwent ostomy surgery in 2005. Six days later, the nurse reported that during the removal procedure of the convatec loop ostomy rod, the ostomy rod "broke". The nurse was able to retrieve the missing piece which prevented the patient from returning back to the or.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1049092-2005-00030
MDR Report Key599863
Report Source05
Date Received2005-05-02
Date of Report2005-05-02
Date of Event2005-04-18
Date Mfgr Received2005-04-22
Date Added to Maude2005-05-10
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 ContactADRIENNE MCNALLY
Manufacturer Street200 HEADQUARTERS PARK DRIVE
Manufacturer CitySKILLMAN NJ 08858
Manufacturer CountryUS
Manufacturer Postal08858
Manufacturer Phone9089042630
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCONVATEC LOOP OSTOMY ROD
Generic NameOSTOMY ROD
Product CodeEZP
Date Received2005-05-02
Model Number*
Catalog Number22355
Lot NumberUNK
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key589703
ManufacturerCONVATEC,
Manufacturer Address200 HEADQUATERS PARK DRIVE SKILLMAN NJ 08558 US
Baseline Brand NameCONVATEC LOOP OSTOMY ROD
Baseline Generic NameOSTOMY ROD
Baseline Model NoNA
Baseline Catalog No22355
Baseline IDNA
Baseline Device FamilyOSTOMY ROD
Baseline Shelf Life ContainedN
Baseline Shelf Life [Months]*
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK811240
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2005-05-02

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