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
NACatalog 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