FDA Adverse Event Death Summary report: N

NC EMERGE®

MDR report key: 6196447 · Received December 21, 2016

Report

Report Number
2134265-2016-11341
Event Type
Death
Date Received
December 21, 2016
Date of Event
November 18, 2016
Report Date
November 21, 2016
Manufacturer
BOSTON SCIENTIFIC - MAPLE GROVE
Product Code
LOX
PMA / PMN Number
K141236
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KY, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

DEVICE EVALUATED BY MFR: THE DEVICE WAS NOT RETURNED FOR ANALYSIS. THE MANUFACTURING BATCH RECORD REVIEW CONFIRMED THAT THE DEVICE MET ALL MATERIAL, ASSEMBLY AND PERFORMANCE SPECIFICATIONS. THE ROOT CAUSE IS ANTICIPATED PROCEDURAL COMPLICATIONS AS THIS EVENT IS A KNOWN PHYSIOLOGICAL EFFECT OF THE PROCEDURE AND IS NOTED WITHIN THE DFU. (B)(4).

Description of Event or Problem · 1

SAME CASE AS MDR ID: 2134265-2016-11337; 2134265-2016-11338; 2134265- 2016-11355; 2134265-2016-11342; 2134265-2016-11339; 2134265-2016-11340; 2134265-2016-11343; 2134265-2016-11336; 2134265-2016 -11380; 2134265-2016-11378; 2134265-2016-11379. IT WAS REPORTED THAT PATIENT DEATH OCCURRED. THE TARGET LESION WAS LOCATED IN THE LEFT ANTERIOR DESCENDING ARTERY. DURING TESTING OF A 1.50MM ROTALINK¿ PLUS AND ROTAWIRE GUIDE WIRE WITH THE ROTABLATOR CONSOLE AND A DYNAGLIDE FOOT PEDAL, THE SYSTEM BASELINE TESTED "OKAY" OUTSIDE THE PATIENT. ROTATIONAL ATHERECTOMY WAS PERFORMED HOWEVER, THE BURR STOPPED SPINNING AND A HISSING NOISE WAS NOTED FROM THE NITROGEN TANK TO THE CONSOLE. IT WAS FURTHER REPORTED ATHERECTOMY WAS DISCONTINUED AND SEVERAL BOSTON SCIENTIFIC BALLOONS AND STENTS WERE UTILIZED. THE PATIENT EXPIRED. ADDITIONAL INFORMATION WAS REQUESTED BUT NOT AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
842766 NC EMERGE® CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS LOX BOSTON SCIENTIFIC - MAPLE GROVE H7493926720250 19767001

Patients

Seq Age Sex Outcome Treatment
1 Death