FDA Adverse Event Injury Summary report: N

BRK-1? XS TRANSSEPTAL NEEDLE, 71 CM LENGTH

MDR report key: 4130146 · Received September 30, 2014

Report

Report Number
3005188751-2014-00114
Event Type
Injury
Date Received
September 30, 2014
Date of Event
August 11, 2014
Report Date
September 5, 2014
Manufacturer
ST. JUDE MEDICAL, INC. (AF-MINNETONKA)
Product Code
DRC
PMA / PMN Number
PK072278
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE RESULTS OF THE INVESTIGATION ARE INCONCLUSIVE SINCE THE DEVICE WAS NOT RETURNED FOR ANALYSIS. OUR INVESTIGATION WAS LIMITED TO THE REVIEW OF THE DEVICE HISTORY RECORD, WHICH SHOWED THAT EACH MANUFACTURING AND INSPECTION OPERATION WAS PERFORMED AND INDICATED COMPLETE IN ACCORDANCE WITH SJM SPECIFICATIONS AND PROCEDURES. BASED ON THE INFORMATION RECEIVED, THE CAUSE OF THE REPORTED CARDIAC PERFORATION COULD NOT BE CONCLUSIVELY DETERMINED. PER THE IFU, CARDIAC PERFORATION IS A KNOWN RISK DURING THE USE OF THIS DEVICE.

Description of Event or Problem · 1

RELATED MANUFACTURER REFERENCE 3005188751-2014-00115. DURING A LEFT ATRIAL MAPPING PROCEDURE USING A BRK TRANSSEPTAL NEEDLE AND AN AGILIS NXT INTRODUCER, A CARDIAC PERFORATION OCCURRED. DURING THE CASE, THE PATIENT BECAME HYPOTENSIVE. AN ICE CATHETER CONFIRMED A LEFT ATRIAL PERFORATION, FOR WHICH A PERICARDIOCENTESIS WAS PERFORMED TO STABILIZE THE PATIENT. THE PATIENT WAS THEN PREPPED FOR TRANSFER TO SURGERY. FURTHER INFORMATION WAS UNAVAILABLE. THERE WERE NO PERFORMANCE ISSUES WITH ANY SJM DEVICE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
607280 BRK-1? XS TRANSSEPTAL NEEDLE, 71 CM LENGTH TRANSSEPTAL NEEDLE DRC ST. JUDE MEDICAL, INC. (AF-MINNETONKA) G407209 4547371

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention AGILIS NXT INTRODUCER| CARTO 3 MAPPING SYSTEM| COOL FLOW PUMP| UNKNOWN BIOSENSE WEBSTER CATHETER| STOCKERT GENERATOR