Teleflex Medical: Medical Device Recall in 2015 - (Recall #: Z-1051-2015)

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:

MAQUET, SERVO Humidifier 163, Rx Only, Inmed Mfg. Sdn Bhd. Catalog No: XKC01-06-8125-8, Model No. 01-06-8125-8. A heat and moisture condenser (artificial 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 humidify gases breathed in by a patient.

Product Classification:

Class I

Date Initiated: January 12, 2015

Date Posted: February 18, 2015

Recall Number: Z-1051-2015

Event ID: 70257

Reason for Recall:

Defects: Cracks that may occur in the center of the corrugated flex tube of the 15 mm and 22 mm ISO female connector.

Status: Terminated

Product Quantity: 100 units

Code Information:

Lot numbers: 201413, 201414, 201415, 201417, 201419 and 201422.

Distribution Pattern:

Distributed to FL, KS, MI and WV.

Voluntary or Mandated:

Voluntary: Firm initiated