Teleflex, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2409-2015)

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:

Bronchial One Lumen Tube - Left

Product Classification:

Class II

Date Initiated: November 21, 2014

Date Posted: August 26, 2015

Recall Number: Z-2409-2015

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 115900-000065 Batch Number 13FT06, 13GT24, 13JT08, 13KT12, 13LT08, 14AT20, 14DT19, 14ET04, 14GT10, 14GT15, 14IT11, 14JT09, 14JT24; Product Code 115900-000080 Batch Number 13FT17, 13IT11, 13KT05, 13KT12, 14AT04, 14BT04, 14BT15, 14DT19, 14ET04, 14ET22, 14GT15, 14GT18, 14IT14, 14JT09, 14JT18

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