FDAFebruary 11, 2019device

Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula comes inside a package which is labeled in part, Product Usage: The Portex Blue Line Ultra¿ Tracheostomy Tubes are indicated for airway maintenance of tracheostomized patients.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Packaged with an incorrect size inner cannula.

What to do

FDA enforcement status: Terminated

Brands named

smiths medical asdsmithssmiths medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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