CONTOUR EMBOLIZATION PARTICLES 760082

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 1999-10-14 for CONTOUR EMBOLIZATION PARTICLES 760082 manufactured by Target Therapeutics/a Div Of Boston Scientific Corp..

Event Text Entries

[160636] It was reported to target that the contents of the vial looked too fine. This event did not affect the pt because it was observed during preparation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number6000078-1999-00091
MDR Report Key245514
Report Source01,05
Date Received1999-10-14
Date of Report1999-10-14
Date of Event1999-06-08
Date Mfgr Received1999-06-08
Device Manufacturer Date1999-02-01
Date Added to Maude1999-10-22
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
Manufacturer ContactCARMEN ORELLANA
Manufacturer Street47900 BAYSIDE PKWY
Manufacturer CityFREMONT CA 945386515
Manufacturer CountryUS
Manufacturer Postal945386515
Manufacturer Phone8006622415
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionRC
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCONTOUR EMBOLIZATION PARTICLES
Generic NameEMBOLIZATION PARTICLES
Product CodeMZQ
Date Received1999-10-14
Returned To Mfg1999-06-24
Model NumberNA
Catalog Number760082
Lot NumberA74000
ID NumberNA
Device Expiration Date2002-01-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagY
Date RemovedA
Device Sequence No1
Device Event Key237865
ManufacturerTARGET THERAPEUTICS/A DIV OF BOSTON SCIENTIFIC CORP.
Manufacturer Address479000 BAYSIDE PKWY. FREMONT CA 945386515 US
Baseline Brand NameCONTOUR EMBOLIZATION PARTICLES
Baseline Generic NamePVA
Baseline Model NoNA
Baseline Catalog No760082
Baseline IDNA
Baseline Device FamilyCONTOUR
Baseline Shelf Life Contained*
Baseline Shelf Life [Months]36
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK914866
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 1999-10-14

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