FDA Adverse Event Malfunction Summary report: N

HYDRO THERMABLATOR (HTA) ENDOMETRIAL ABLATION SYSTEM

MDR report key: 3062663 · Received April 17, 2013

Report

Report Number
3005099803-2013-02481
Event Type
Malfunction
Date Received
April 17, 2013
Report Date
March 22, 2013
Manufacturer
BOSTON SCIENTIFIC - FREMONT (CE)
Product Code
MNB
PMA / PMN Number
P000040
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

ANALYSIS OF THE RETURNED HYDRO THERMABLATOR (HTA) ENDOMETRIAL ABLATION SYSTEM REVEALED THE UNIT PASSED A SAFETY AND CURRENT TEST. THE POWER CORD WAS WIGGLED AT THE RECEPTACLE OF THE UNIT DURING THE TESTING TO TRY AND DUPLICATE THE REPORTED PROBLEM. THE CONSOLE WAS OPENED AND VISUALLY INSPECTED FOR LOOSE CONNECTIONS AND LOOSE OR MISSING HARDWARE. NO LOOSE CONNECTIONS OR LOOSE OR MISSING HARDWARE WAS FOUND. FURTHERMORE, THIS EVENT IS DETERMINED TO NOT BE MDR REPORTABLE.

Description of Event or Problem · 1

IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A HYDRO THERMABLATOR (HTA) ENDOMETRIAL ABLATION SYSTEM WAS BEING INSPECTED BY THE BIOMEDICAL DEPARTMENT PRIOR TO A PROCEDURE ON AN UNKNOWN DATE. ACCORDING TO THE COMPLAINANT, THE UNIT FAILED THE GROUNDING TEST DUE TO A LOOSE POWER CORD. THERE WAS NO PATIENT INVOLVED

Description of Event or Problem · 1

IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A HYDRO THERMABLATOR (HTA) ENDOMETRIAL ABLATION SYSTEM WAS BEING INSPECTED BY THE BIOMEDICAL DEPARTMENT PRIOR TO A PROCEDURE ON AN UNKNOWN DATE. ACCORDING TO THE COMPLAINANT, THE UNIT FAILED THE GROUNDING TEST DUE TO A LOOSE POWER CORD. THERE WAS NO PATIENT INVOLVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
166112 HYDRO THERMABLATOR (HTA) ENDOMETRIAL ABLATION SYSTEM DEVICE, THERMAL ABLATION, ENDOMETRIAL MNB BOSTON SCIENTIFIC - FREMONT (CE) M00658001R0

Patients

Seq Age Sex Outcome Treatment
1