FDA Adverse Event Malfunction Summary report: N

JAGWIRE?

MDR report key: 4122573 · Received September 26, 2014

Report

Report Number
3005099803-2014-03229
Event Type
Malfunction
Date Received
September 26, 2014
Date of Event
September 4, 2014
Report Date
September 5, 2014
Manufacturer
BOSTON SCIENTIFIC - COSTA RICA (COYOL)
Product Code
EZB
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CN
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4) GUIDEWIRE DISTAL TIP DETACHED EXPOSING THE TIP OF THE METAL COREWIRE. THE DEVICE HAS NOT BEEN RECEIVED FOR ANALYSIS. UPON RECEIPT AND COMPLETION OF THE FAILURE ANALYSIS OF THE COMPLAINT DEVICE, IF THERE IS ANY FURTHER RELEVANT INFORMATION FROM THAT REVIEW, A SUPPLEMENTAL MEDWATCH WILL BE FILED.

Description of Event or Problem · 1

NOTE: THIS REPORT PERTAINS TO ONE OF SIX DEVICES THAT WERE INSPECTED. REFER TO MANUFACTURER REPORT #3005099803-2014-03227, 3005099803-2014-03228, 3005099803-2014-03229, 3005099803-2014-03230, 3005099803-2014-03231 AND 3005099803-2014-03232 FOR THE OTHER ASSOCIATED DEVICE INFORMATION. IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A JAGWIRE GUIDEWIRE WAS INSPECTED. ACCORDING TO THE COMPLAINANT, SINCE THE EVENT, HYDROPHILIC TIP DETACHED, OCCURRED SEVERAL TIMES, THE USER UNPACKED THE JAGWIRE GUIDEWIRE AND FOUND THAT THE HYDROPHILIC TIP WAS DETACHED EXPOSING THE TIP OF THE METAL COREWIRE. FIVE MORE JAGWIRE GUIDEWIRES WERE OPENED AND THE HYDROPHILIC TIP ALSO DETACHED EXPOSING THE TIP OF THE METAL COREWIRE. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION REGARDING THE CIRCUMSTANCES SURROUNDING THIS EVENT HAVE BEEN UNSUCCESSFUL TO DATE. SHOULD ADDITIONAL RELEVANT DETAILS BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
600438 JAGWIRE? STYLET FOR CATHETER, GASTRO-UROLOGY EZB BOSTON SCIENTIFIC - COSTA RICA (COYOL) M0055658011 16293728

Patients

Seq Age Sex Outcome Treatment
1