PROLIEVE THERMODILITATION SYSTEM M0068808260

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 2011-12-14 for PROLIEVE THERMODILITATION SYSTEM M0068808260 manufactured by Boston Scientific - Marlborough.

Event Text Entries

[2507400] It was reported to boston scientific corporation (bsc) that a patient underwent a procedure with a prolieve thermodilatation kit for the treatment of benign prostatic hyperplasia (bph). It was reported that the thermal balloon did not deflate. According to the bsc sales representative, the physician reported he had difficulty deflating the thermal balloon. Follow up with the complainant revealed that at procedure closure when the physician went to deflate the compression balloon, it would not deflate. He then pulled out the catheter to remove it. He had to use a tamponade catheter to stop the bleeding. The catheter was in place until the next day. The patient is doing well.
Patient Sequence No: 1, Text Type: D, B5


[9578572] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3005099803-2011-04179
MDR Report Key2373801
Report Source05,07
Date Received2011-12-14
Date of Report2011-11-21
Date of Event2011-11-17
Date Mfgr Received2011-11-21
Device Manufacturer Date2011-07-28
Date Added to Maude2011-12-14
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 FDA0
Event Location0
Manufacturer ContactEMP. CHARLES MONTGOMERY
Manufacturer Street100 BOSTON SCIENTIFIC WAY
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Manufacturer Phone5086834000
Manufacturer G1ACCELLENT ENDOSCOPY JUAREZ
Manufacturer Street31C BUTTERFIELD TRAIL
Manufacturer CityEL PASO TX 79906
Manufacturer CountryUS
Manufacturer Postal Code79906
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePROLIEVE THERMODILITATION SYSTEM
Generic NameSYSTEM, HYPERTHERMIA, RF/MICROWAVE (BENIGN PROSTATIC HYPERPLASIA),THERMOTHERAPY
Product CodeMEQ
Date Received2011-12-14
Model NumberM0068808260
Lot Number0000878865
Device Expiration Date2013-06-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC - MARLBOROUGH
Manufacturer Address100 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2011-12-14

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