GALAXY INTRAVASCULAR ULTRASOUND SYSTEM
Report
- Report Number
- 2134265-2013-03105
- Event Type
- Malfunction
- Date Received
- May 9, 2013
- Date of Event
- April 11, 2013
- Report Date
- April 11, 2013
- Manufacturer
- BOSTON SCIENTIFIC - FREMONT (SUD)
- Product Code
- IYO
- PMA / PMN Number
- K980851
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IT
- Reporter Occupation
- PHYSICIAN
Narratives
DEVICE EVALUATED BY MANUFACTURER: 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).
SAME CASE AS MDR ID 2134265-2013-03104 , MDR ID 2134265-2013-03106. IT WAS REPORTED THAT DURING INTRAVASCULAR ULTRASOUND (IVUS), FAILURE TO PULLBACK OCCURRED. THE PHYSICIAN USED AN ILAB CART SYSTEM 240 WITH A BSC CORONARY IMAGING CATHETER AND ASSY SLED PULLBACK SINGLE PACK MD5 TO IMAGE AN UNSPECIFIED VESSEL. DURING THE PROCEDURE, AN MDU OVERLOAD ERROR OCCURRED. THE PULLBACK WOULD NOT WORK AND THE MDU WOULD NOT MOVE AT ALL. THE PHYSICIAN ATTEMPTED AUTOMATIC PULLBACK 3 TIMES AND TRIED TO CHECK THE MDU CONNECTIONS WITHOUT SUCCESS. MANUAL PULLBACK WAS PERFORMED AND THE PROCEDURE WAS COMPLETED WITH A DIFFERENT DEVICE WITHOUT FURTHER IVUS USE. IT HAS BEEN NOTED THAT NO PATIENT COMPLICATIONS WERE REPORTED AND PATIENT'S CONDITION IS STABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 202964 | GALAXY INTRAVASCULAR ULTRASOUND SYSTEM | SYSTEM, IMAGING, PULSED ECHO, ULTRASONIC | IYO | BOSTON SCIENTIFIC - FREMONT (SUD) | H749A70200 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |