Teleflex Medical: Medical Device Recall in 2017 - (Recall #: Z-1177-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A tracheal tube is inserted into a patients mouth or nose for airway management

Product Classification:

Class II

Date Initiated: October 18, 2016

Date Posted: February 15, 2017

Recall Number: Z-1177-2017

Event ID: 76133

Reason for Recall:

Labeling inconsistency - units labeled with a 7mm tube may contain a size 6.5mm tube, and units labeled 7.5mm tube may contain a size 5.5mm tube.

Status: Terminated

Product Quantity: 25,274 units

Code Information:

Lots 73A1500461 & 73D1400082

Distribution Pattern:

Worldwide Distribution - US including AL, AZ, ARK, CA, CO, CT, FL, GA. HI, KS, KY, IL, IN, IA, LA, MD, MA, MI, MN, MS, MO, MT, NE, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WV and Internationally to Canada, Chile, & Japan

Voluntary or Mandated:

Voluntary: Firm initiated