Teleflex, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2413-2015)

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:

Tracheopart Set (Right), Sterile

Product Classification:

Class II

Date Initiated: November 21, 2014

Date Posted: August 26, 2015

Recall Number: Z-2413-2015

Event ID: 71727

Reason for Recall:

Customer complaints reporting that the cobb connector detached from the main connector prior to use.

Status: Terminated

Product Quantity:

Code Information:

Product Code 116401-000750 Batch Number 13FT06, 13GT24, 13JT21, 13IT21R, 13KT23, 13KT23R, 14CT21, 14ET11, 14ET22, 14ET28, 14FT16, 14GT15, 14GT23, 14IT17, 14JT18; Product Code 116401-000850 Batch Number 13IT05, 13IT21R, 13KT05, 13LT08, 14CT16, 14DT19, 14ET10, 14ET22, 14FT16, 14GT05, 14GT18, 14HT03, 14HT09; Product Code 116401-000950 Batch Number 13JT21R, 14CT06, 14CT16, 14DT20, 14ET23, 14FT04, 14GT05, 14GT18, 14HT17, 14IT08

Distribution Pattern:

AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago

Voluntary or Mandated:

Voluntary: Firm initiated