3.5F BETA-RAIL DELIVERY CATHETER ABR 6001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2004-02-19 for 3.5F BETA-RAIL DELIVERY CATHETER ABR 6001 manufactured by Novoste Corp..

Event Text Entries

[365221] The distal tip of the catheter got stuck at the treatment site. The catheter stuck on the guidewire and pulled out together with the guidewire causing a dissection of the proximal lad. The dr. Placed a stent at the dissected site and continued normal ptca. The pt is doing fine.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1062385-2004-00003
MDR Report Key526288
Report Source05,07
Date Received2004-02-19
Date of Report2004-02-19
Date of Event2004-01-27
Date Mfgr Received2004-02-15
Date Added to Maude2004-05-25
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 ContactADAM LOWE, VP
Manufacturer Street3890 STEFE REYNOLDS BLVD.
Manufacturer CityNORCROSS GA 30093
Manufacturer CountryUS
Manufacturer Postal30093
Manufacturer Phone7707170904
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name3.5F BETA-RAIL DELIVERY CATHETER
Generic NameCATHETER
Product CodeMOU
Date Received2004-02-19
Returned To Mfg2004-02-15
Model NumberNA
Catalog NumberABR 6001
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key515443
ManufacturerNOVOSTE CORP.
Manufacturer Address3890 STEVE REYNOLDS BLVD. NORCROSS GA 30093 US
Baseline Brand Name3.5F BETA-RAIL DELIVERY CATHETER
Baseline Generic NameCATHETER
Baseline Model NoNA
Baseline Catalog NoABR 6001
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2004-02-19

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