FDA Adverse Event Injury Summary report: N

NRG TRANSSEPTAL NEEDLE

MDR report key: 11057644 · Received December 22, 2020

Report

Report Number
9710452-2020-00053
Event Type
Injury
Date Received
December 22, 2020
Report Date
December 22, 2020
Manufacturer
BAYLIS MEDICAL COMPANY INC.
Product Code
DXF
PMA / PMN Number
K073326
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS MDR IS BEING REPORTED ACCORDING TO THE TIMELINES SPECIFIED PER THE FDA GUIDANCE FOR INDUSTRY "POSTMARKETING ADVERSE EVENT REPORTING FOR MEDICAL PRODUCTS AND DIETARY SUPPLEMENTS DURING A PANDEMIC" (MAY 2020), FOLLOWING FDA NOTIFICATION OF THE DEFERRED REPORTING.

Description of Event or Problem · 1

DURING A LITERATURE REVIEW, AN ARTICLE [1] WAS IDENTIFIED IN WHICH ONE PATIENT HAD HYPOTENSION REQUIRING VASOACTIVE MEDICATIONS AND ONE HAD CEREBROVASCULAR ACCIDENT FOLLOWING THE PULMONARY VEIN ISOLATION PROCEDURE IN WHICH THE NRG TRANSSEPTAL NEEDLE WAS USED AMONG OTHER DEVICES, INCLUDING SL1 (ABBOTT), PREFACE SHEATH (BIOSENSE WEBSTER), ARCTIC FRONT ADVANCE (MEDTRONIC) AND CRYOSHEATH (MEDTRONIC). THERE IS NO EVIDENCE TO SUGGEST THAT THE BAYLIS MEDICAL DEVICE CAUSED OR CONTRIBUTED TO THE REPORTED INCIDENT. HOWEVER, AS A BAYLIS MEDICAL DEVICE WAS REPORTED TO BE AMONG THE DEVICES USED IN THE PROCEDURE, BAYLIS MEDICAL HAS DECIDED TO SUBMIT THIS REPORT. [1] PEIGH, G., KAPLAN, R. M., BAVISHI, A., DIAZ, C. L., BAMAN, J. R., MATIASZ, R., . . . PASSMAN, R. S. (2019). A NOVEL RISK MODEL FOR VERY LATE RETURN OF ATRIAL FIBRILLATION BEYOND 1 YEAR AFTER CRYOBALLOON ABLATION: THE SCALE-CRYOAF SCORE. J INTERV CARD ELECTROPHYSIOL. DOI:10.1007/S10840-019-00588-X.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1520968 NRG TRANSSEPTAL NEEDLE RF TRANSSEPTAL NEEDLE DXF BAYLIS MEDICAL COMPANY INC.

Patients

Seq Age Sex Outcome Treatment
1 Life Threatening