FDA recall record

Smiths Medical ASD Bivona Mid-Range Aire-Cuf Adult Tracheostomy Tube This tube is intended recall — FDA Z-2946-2020

Label has the incorrect size for the tracheotomy tube.

Class IIclassification
Z-2946-2020official record ID
Sep 16, 2020report date

Recall record at a glance

Official recordZ-2946-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSmiths Medical ASD Inc.
Report dateSep 16, 2020
Recall initiation dateAug 28, 2020
Quantity3 units
LocationMinneapolis, MN, United States

Official product description

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.

Why the product was recalled

Label has the incorrect size for the tracheotomy tube.

Distribution information

US Distribution to state of: CT

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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