Teleflex Medical: Medical Device Recall in 2015 - (Recall #: Z-0419-2016)

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 Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column

Product Classification:

Class II

Date Initiated: April 17, 2014

Date Posted: December 23, 2015

Recall Number: Z-0419-2016

Event ID: 72731

Reason for Recall:

Product is being recalled due to complaints that the inspiratory and expiratory tubes are transposed.

Status: Terminated

Product Quantity: 2,600 ea

Code Information:

Lot Numbers : 02K1300128 and 02L1302324

Distribution Pattern:

US Distribution to the states of : AL, AZ, CA, GA, IL, KY, LA, MA, MI, MN, NJ, NY, NC, OH, OK, OR, PA, TN, TX and WA.

Voluntary or Mandated:

Voluntary: Firm initiated