Balloon dilation complication during the treatment of subglottic stenosis: background of the FDA class 1 recall for the 18 x 40-mm Acclarent Inspira AIR balloon dilation system

Ann Otol Rhinol Laryngol. 2013 Jun;122(6):364-8. doi: 10.1177/000348941312200603.

Abstract

Objectives: Balloon dilation for subglottic stenosis allows for a controlled radial expansion of the airway and is considered superior to older techniques of airway dilation. We report the case of a 39-year-old woman with idiopathic subglottic stenosis who had entrapment of an inflated balloon in her subglottis due to device failure while undergoing balloon dilation of the stenotic area.

Methods: We present a case report and a review of the literature.

Results: As a result of this and other reported incidents, on March 13, 2012, the US Food and Drug Administration issued a class 1 recall of the 18 x 40-mm Acclarent Inspira AIR Balloon Dilation System (Acclarent Inc, Menlo Park, California).

Conclusions: This is the first report describing a dislodged inflated balloon in the subglottis as a complication of dilation for idiopathic subglottic stenosis. Awareness of this possibility, as well as preparedness with the proper instruments, is vital for prevention of a catastrophic emergency during an otherwise low-risk procedure.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Dilatation / adverse effects*
  • Dilatation / methods
  • Endoscopy / methods*
  • Equipment Failure
  • Female
  • Humans
  • Laryngostenosis / therapy*
  • Medical Device Recalls*
  • United States
  • United States Food and Drug Administration