Teleflex Medical: Medical Device Recall in 2016 - (Recall #: Z-2374-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Servo Humidifier 163, Model 01-06-8125-8, REF 6419365 Product Usage: A heat and moisture condenser (artifical nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tube (a tube inserted into the trachea) to warm and humidity gases breathed in by the patient.

Product Classification:

Class II

Date Initiated: December 3, 2015

Date Posted: August 17, 2016

Recall Number: Z-2374-2016

Event ID: 74681

Reason for Recall:

Cracks may occur at the 15mm and 22mm ISO female connector.

Status: Terminated

Product Quantity: 2,700 ea.

Code Information:

Lots 201450, 201451, 201452, 201504

Distribution Pattern:

US Nationwide Distribution in the states of FL, KS and WV.

Voluntary or Mandated:

Voluntary: Firm initiated