Teleflex Medical: Medical Device Recall in 2015 - (Recall #: Z-1078-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Hudson RCI, Sheridan, Preformed Tracheal Tubes, Cuffed and Uncuffed, Rx Only, Sterile, Teleflex Medical.

Product Classification:

Class II

Date Initiated: January 9, 2015

Date Posted: February 18, 2015

Recall Number: Z-1078-2015

Event ID: 70248

Reason for Recall:

Labeling; The affected product packaging is incorrectly labeled as being a cuffed oral ET tube; The correct product labeling is uncuffed nasal ET tube.

Status: Terminated

Product Quantity: 300 units

Code Information:

Catalog no. 5-22110, Lot no. 01M1300076.

Distribution Pattern:

Worldwide Distribution - US Distribution to the states of FL, GA, IL, KY, MA, MI, MO, MS, OH, TX, WA and WV., and to the countries of Canada and the Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated