Teleflex, Inc. recalls Bronchial Double Lumen Tube Set (Left), Sterile

Recall date

November 21, 2014

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2407-2015

FDA classification

Class II

Brand / firm

Teleflex, Inc.

Sold / distributed

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

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Bronchial Double Lumen Tube Set (Left), Sterile