FDA Adverse Event Malfunction Summary report: N

ILAB ULTRASOUND IMAGING SYSTEM

MDR report key: 2962616 · Received February 14, 2013

Report

Report Number
2134265-2013-00512
Event Type
Malfunction
Date Received
February 14, 2013
Date of Event
January 15, 2013
Report Date
January 16, 2013
Manufacturer
BOSTON SCIENTIFIC - FREMONT (CE)
Product Code
IYO
PMA / PMN Number
K051679
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AU
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). DEVICE EVALUATED BY MFR.: IT IS INDICATED THAT THE DEVICE WILL NOT BE RETURNED FOR EVALUATION; THEREFORE, A FAILURE ANALYSIS OF THE COMPLAINT DEVICE COULD NOT BE COMPLETED. A REVIEW OF THE BATCH HISTORY, HISTORICAL TRENDING, AND SIMILAR COMPLAINT TRENDING REVIEW FOR THE PRODUCT FAMILY WILL BE CONDUCTED. IF THERE IS ANY FURTHER RELEVANT INFORMATION FROM THAT REVIEW, A SUPPLEMENTAL MEDWATCH WILL BE FILED. (B)(4).

Description of Event or Problem · 1

SAME CASE AS MDR ID # 2134265-2013-00511, 2134265-2013-00513. IT WAS REPORTED THAT DURING ANGIOPLASTY PROCEDURE, THE ILAB SYSTEM AUTOMATIC PULLBACK STOPPED. DURING THE PROCEDURE THE PHYSICIAN STARTED A MOTOR DRIVE UNIT (MDU) PULLBACK OF THE ILAB SYSTEM. HE NOTICED THAT THE IMAGE DID NOT MOVE AND SLIGHT SQUEALING SOUND CAME FROM THE SLED AND THE PULLBACK STOPPED. THEN HE TRIED ANOTHER PULLBACK AFTER MAKING SURE THE MDU WAS CORRECTLY CONNECTED TO THE SLED. IT WAS UNABLE TO PULLBACK AND THE SQUEALING SOUND GOT LOUDER. THEY DISCONNECTED THE MDU FROM THE SLED AND NOTICED THAT THE SQUEALING SOUND STOPPED. THE PROCEDURE WAS COMPLETED WITH THE MANUAL PULLBACK. NO PATIENT COMPLICATIONS WERE REPORTED AND THE PATIENT STATUS IS STABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
64686 ILAB ULTRASOUND IMAGING SYSTEM CATHETER, ULTRASOUND, INTRAVASCULAR IYO BOSTON SCIENTIFIC - FREMONT (CE) UNK71

Patients

Seq Age Sex Outcome Treatment
1