Teleflex Medical: Medical Device Recall in 2016 - (Recall #: Z-1938-2016)

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:

Sterile Sheridan/HVT Cuffed, Murphy Eye, Tracheal Tube, Ref: V5-10314, ID: 7.0 mm, Rx Only, Manufactured by: Teleflex Incorporated. A tracheal tube is inserted into a patients mouth or nose for airway management.

Product Classification:

Class II

Date Initiated: May 5, 2016

Date Posted: June 15, 2016

Recall Number: Z-1938-2016

Event ID: 74034

Reason for Recall:

The labeling of some units indicates that it contains a size 7mm tracheal tube, but may contain a size 7.5mm tracheal tube.

Status: Terminated

Product Quantity: 6,390 ea.

Code Information:

Lot 73F1500606

Distribution Pattern:

US Distribution to states of: AL, AZ, CO, FL, GA, ID, IL, IN, IA, KY, LA, MD, MA, MI, MN, MO, NY, NC, OK, PA, RI, TX and UT.

Voluntary or Mandated:

Voluntary: Firm initiated