* 322-24

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1998-03-23 for * 322-24 manufactured by Dow Corning Corp/ Medical Products.

Event Text Entries

[18552975] On 3/10/1998, md attempted to remove suprapublic malecot catheter. This was placed in o. R. On 2/14/1998. The tip of catheter broke off internally. Retained section was surgically removed during exploration on 3/10/1998.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number159310
MDR Report Key159310
Date Received1998-03-23
Date of Report1998-03-18
Date of Event1998-03-10
Date Facility Aware1998-03-10
Report Date1998-03-18
Date Reported to FDA1998-03-20
Date Reported to Mfgr1998-03-20
Date Added to Maude1998-03-27
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
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 Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand Name*
Generic NameSILICONE MALECOT SUPRAPUBIC CATHETER
Product CodeFEW
Date Received1998-03-23
Model Number*
Catalog Number322-24
Lot Number*
ID Number24FR 25CM SILICONE THREE WING
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeUNKNOWN
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key155167
ManufacturerDOW CORNING CORP/ MEDICAL PRODUCTS
Manufacturer Address* MIDLAND MI 48640 US
Baseline Brand NameSILASTIC MALECOT CATHETER
Baseline Generic NameMALECOT CATHETER
Baseline Model NoNA
Baseline Catalog No322-24
Baseline IDNA
Baseline Device FamilyDRAIN, MALECOT
Baseline Shelf Life Contained*
Baseline Shelf Life [Months]*
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1998-03-23

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