Teleflex Medical: Medical Device Recall in 2014 - (Recall #: Z-2107-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Hudson RCI, Breathing Circuit, Adult, Single Limb w/Heated Wire, [Respiratory Gas Humidifier, (Direct Patient Interface)]. The Hudson Heated Wire Ventilator Circuit is intended as a conduit for respiratory gas between a patient and a ventilator, and includes heated wires for use with a Concha Column Humidifier.

Product Classification:

Class II

Date Initiated: July 9, 2014

Date Posted: July 30, 2014

Recall Number: Z-2107-2014

Event ID: 68731

Reason for Recall:

The temperature probe does not properly connect to the temperature port.

Status: Terminated

Product Quantity: 11,679 units

Code Information:

Catalog Number: 780-96, Lot numbers: 02L1300073 & 02A140133.

Distribution Pattern:

Worldwide Distribution - US including the states of CA, FL, KS, KY, MA, MI, MO, NC, NE, NJ, NY, OH, PA, TN, TX and VA, and the countries of Argentina, Chile, Colombia, and the Philippines

Voluntary or Mandated:

Voluntary: Firm initiated