ClearanceBrief
Recall Z-1466-2010 ยท JOH Tube Tracheostomy And Tube Cuff

Nellcor Puritan Bennett Inc. (dba Covidien Ltd)

Shiley Fenestrated Low Pressure Cuffed Tracheostomy Tube, 4 FEN, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Intended for bypass of upper airway obstructions, provide long term ventilation, support and/or manage tracheal/bronchial secretions.

DateMay 6, 2010 (initiated Apr 13, 2010)
StatusTerminated
ReasonInflatable cuff Tracheostomy tubes may leak air, resulting in inadequate ventilation.
Root causeProcess design
ActionCovidien issued an "Urgent Medical Device Recall" notification dated April 13, 2010. Consignees were alerted to the affected device. If an affected product is already in use, the firm recommends that the tube be replaced as soon as the patient's physician determines it is clinically appropriate. All affected product is to be returned to the firm. For further Information, contact Covidien at 1-800-635-5267.
Quantity5,076 units
DistributionWorldwide Distribution -- United States (including Guam and Puerto Rico), Australia, Belgium, Brazil, Canada, Chile, Colombia, Honduras, Japan, Mexico, Panama, Singapore and Uruguay.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K962173SHIKEY TRACHEOSTOMY TUBES AND ACCESSORIES
Mallinckrodt Medical, Oct 4, 1996