inforMED
InjuryKAM

RELIEVA SINUS BALLOON CATHETER SYSTEM

Received Apr 11, 2014

Report 3005172759-2014-00009 · MDR key 3761017

Device

Generic name

Sinus Balloon Catheter

Manufacturer

Acclarent, Inc.

Model number

NA

Catalog number

UNK

Lot number

UNK

Product problems

  • Adverse Event Without Identified Device or Use Problem

Patient

UNK

  • Cerebrospinal Fluid Leakage

Narrative

Additional Manufacturer Narrative

VP OF MEDICAL AFFAIRS REVIEWED THE POST AND CONCLUDED THAT THERE WAS NOT ENOUGH INFORMATION TO KNOW IF THE ACCLARENT DEVICES WERE PART OF THE SURGERY. THE POST INDICATED THAT THE PT HAD BALLOON SINUPLASTY PROCEDURE BUT THERE ARE MANY SURGEONS USING ANY BALLOON FROM ANY MFR AND USE BALLOON SINUPLASTY THIS TERM. PER VP OF MEDIAL AFFAIRS COMMENT, IT IS HIGHLY CSF LEAK. MORE LIKELY IS THAT THE CASE WAS HYBRID CASE (BALLOON SINUPLASTY PROCEDURE PLUS TRADITIONAL TOOLS). ACCLARENT REGIONAL MGR CONFIRMED THAT THERE WERE NO CSF LEAK EVENTS THAT SHE WAS AWARE OF. THERE ARE NO EVIDENCES THAT THE ACCLARENT DEVICES CAUSE OR CONTRIBUTE TO THE REPORTED EVENT. THIS REPORT IS BEING SUBMITTED IN AN ABUNDANCE OF CAUTION. THE SUBJECT DEVICE OF THIS REPORT WAS NOT RETURNED FOR EVALUATION, AND ITS WHEREABOUTS ARE UNK. ACCLARENT WILL CONTINUE TO MONITOR THIS PHENOMENON FOR TRENDING PURPOSES.

Description of Event or Problem

ACCLARENT WAS MADE AWARE OF THIS EVENT ON 03-31-2014 WHEN A COMMENT WAS POSTED ON THE ACCLARENT (B)(4). THE COMMENT MENTIONED THAT THE PT HAD THE BALLOON SINUPLASTY PROCEDURE BY A PHYSICIAN IN (B)(6). FEW DAYS AFTER THE PROCEDURE, THE PT WAS ADMITTED TO (B)(6) WITH A CEREBROSPINAL FLUID LEAK CAUSED BY THE PHYSICIAN, WHO PERFORATED THE ETHMOID ROOF. THE HEAD AND NECK SURGEON MADE A PATCH FROM THE BEHIND THE PT'S EAR AND PATCH IS HEALING NICELY BUT NOW THE PT ALLEGED EXPERIENCING VISION PROBLEM.

Remedial action

  • Other