Smiths Medical ASD Inc.: Medical Device Recall in 2019 - (Recall #: Z-1732-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: February 11, 2019

Date Posted: June 12, 2019

Recall Number: Z-1732-2019

Event ID: 82387

Reason for Recall:

Packaged with an incorrect size inner cannula.

Status: Terminated

Product Quantity: 7,840

Code Information:

Item code/product number: 100/856/080 lot number: 3578884

Distribution Pattern:

Worldwide Distribution - US Nationwide AL, CA, CT, FL, IL, KY, MA, MD, NC, NJ, OH, OR, PA, RI, SC, TN, UT, and VA. Canada, UK and Ireland

Voluntary or Mandated:

Voluntary: Firm initiated