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 2005-03-17 for CONVATEC LOOP OSTOMY ROD * 22355 manufactured by Convatec.

Event Text Entries

[410605] Nurse risk manager reports during transverse colostomy procedure in 2005, the convatec loop ostomy rod broke into two pieces. The surgeon was inserting the loop at the time it broke. He was able to remove the pieces with no adverse affect to the patient and replaced it with another rod.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1049092-2005-00008
MDR Report Key584549
Report Source05
Date Received2005-03-17
Date of Report2005-03-17
Date of Event2005-02-17
Date Mfgr Received2005-02-17
Date Added to Maude2005-03-25
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 HEADQUATERS PARK DR.
Manufacturer CitySKILLMAN NJ 08558
Manufacturer CountryUS
Manufacturer Postal08558
Manufacturer Phone9089042630
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCONVATEC LOOP OSTOMY ROD
Generic NameOSTOMY ROD
Product CodeEZP
Date Received2005-03-17
Model Number*
Catalog Number22355
Lot Number2D53535
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key574380
ManufacturerCONVATEC
Manufacturer Address200 HEADQUARTERS PARK DRIVE SKILLMANRO NJ * 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
10 2005-03-17

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