ClearanceBrief
Recall Z-1863-2013 ยท KTI Bronchoscope Accessory

Acclarent, Inc.

Inspira AIR Balloon Dilation system. Size 10 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.

DateAug 1, 2013 (initiated Jan 11, 2013)
StatusTerminated
ReasonLabeling correction for all sizes of the Inspira AIR Balloon Dilation System to include additional language and warnings as well as to clarify some instructional steps.
Root causeDevice Design
ActionUrgent Medical Device Labeling correction letters will be sent to all consignees through a delivery system that can track delivery. After CDRH review and corrections, Acclarent began issuing customer notification on August 7, 2013
Quantity2703
DistributionWorldwide Distribution-USA (nationwide) and the countries of Belgium, Canada, and Saudi Arabia.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K090660AIRWAY BALLOON CATHETER INFLATION DEVICE
Acclarent, Inc., Jun 12, 2009
K110218INSPIRA AIR BALLOON DILATION SYSTEM
Acclarent, Inc., Mar 31, 2011