medical Class II Updated 2020-09-16

Smiths Medical ASD Inc. recalls Bivona Mid-Range Aire-Cuf Adult Tracheostomy Tube This tu

Recalled Product

Bivona Mid-Range Aire-Cuf Adult Tracheostomy Tube This tube is intended to provide direct airway access for a tracheotomized patient for up to 29 days. It may be reprocessed up to 10 times for single patient use.


Hazard / Issue

Label has the incorrect size for the tracheotomy tube.

Issued by

FDA

Affected States: CT
Lot/Code Info: Lot# 3952216
View official government recall

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