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Teleflex, Inc. recalls Bronchial One Lumen Tube - Left
Recalled August 26, 2015 · FDA recall Z-2409-2015 · Teleflex
Hazard
Customer complaints reporting that the cobb connector detached from the main connector prior to use. · FDA Class II
Sold at
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
Description
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Product
Bronchial One Lumen Tube - Left
Manufacturer(s)
Teleflex, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →