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Recall Observatory FDA recall evidence

Device product

Bronchial One Lumen Tube - Left

Z-2409-2015

November 21, 2014

Class II

Product summary

Firm
Teleflex, Inc.
Event
Event 71727
Status
Terminated
Classification
Class II
Quantity
Unavailable
Official record key
device-enforcement:Z-2409-2015

Official wording

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

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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