Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bronchial One Lumen Tube - Right Recalled by Teleflex, Inc. Due to Customer complaints reporting that the cobb connector detached...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Teleflex, Inc. directly.
Affected Products
Bronchial One Lumen Tube - Right
Why Was This Recalled?
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Where Was This Sold?
This product was distributed to 39 states: 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
About Teleflex, Inc.
Teleflex, Inc. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report