RELIEVA BALLOON
Received Apr 2, 2013
Report 3005172759-2013-00014 · MDR key 3041993
Device
Generic name
Sinus Balloon Catheter
Manufacturer
Acclarent, Inc.Model number
NACatalog number
UNK
Lot number
UNK
Product problems
- Unintended Movement
Patient
44 YR
- Hematoma
- Visual Disturbances
Narrative
Description of Event or Problem
ACCLARENT WAS MADE AWARE OF THIS EVENT ON (B)(6) 2013 WHEN A LITERATURE SEARCH WAS BEING CONDUCTED BY AN ACCLARENT EMPLOYEE. IN THE ARTICLE, AN ACCLARENT BALLOON SINUPLASTY WAS PERFORMED AND AN ACCLARENT ETHMOID SPACER WAS INSERTED. A SUBPERIOSTEAL HEMATOMA DEVELOPED IN THE ROOF OF THE ORBIT RESULTING IN TEMPORARY DIPLOPIA. THE HEMATOMA WAS LOCATED ONLY IN THE SUBPERIOSTEAL SPACE AT THE ROOF OF ORBIT. THE AUTHORS POSTULATE THAT THE UNUSUAL PERFORATIONS IN THE ANTERIOR ORBITAL ROOF BECAME SHEARED FROM THE PRESSURE OF THE BSP BALLOON TRANSMITTED THROUGH OSTEONEOGENIC THICKENED BONE. THE AUTHORS STATE THAT SUBPERIOSTEAL HEMATOMA ARE UNUSUAL AND OCCUR WITH MINOR TRAUMA AROUND THE ORBIT. HE ALSO STATED THAT THE LOCATION OF THE HEMATOMA IN THE SUPERIOR ORBITAL SUBMUCOSAL SPACE WAS EVIDENCE OF TRAUMA FROM THE BALLOON USE IN THE FRONTAL SINUS. THE ACCLARENT ETHMOID SPACER COULD NOT CONTRIBUTE TO THE PATHOLOGY SINCE THE SPACER WAS A SIGNIFICANT DISTANCE AWAY FROM THE REGION OF THE HEMATOMA. THE SURGEON STATED THAT THERE WAS NO BREACH IN THE BONE OF THE SINUSES. THERE WAS NO INTERVENTION AND THE EYE PROBLEM RESOLVED WITH WATCHFUL WAITING.
Additional Manufacturer Narrative
THE AUTHOR OF THE ARTICLE HAS BEEN CONTACTED BY VP OF MEDICAL AFFAIRS BY PHONE ON (B)(6)2013. THE SURGEON STATED THAT THE LOCATION OF THE HEMATOMA IN THE SUPERIOR ORBITAL SUBMUCOSAL SPACER WAS EVIDENCE OF TRAUMA FROM THE BALLOON USED IN THE FRONTAL SINUS. ACCLARENT ETHMOID SPACER COULD NOT CONTRIBUTE TO THE EVENT SINCE THE SPACER WAS SIGNIFICANT DISTANCE AWAY FROM THE REGION OF THE HEMATOMA. THE SURGEON STATED THAT NO TREATMENT OR INTERVENTION AND THE EYE PROBLEM RESOLVED WITH NO SEQUELAE. 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 UNKNOWN. ACCLARENT WILL CONTINUE TO MONITOR THIS PHENOMENON FOR TRENDING PURPOSES.
Remedial action
- Other