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Halyard Health recalls KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.5 mm, Distributed by Kimberly Clark Global Sales, LLC.
Recalled December 31, 2014 · FDA recall Z-0866-2015 · Halyard Health
Hazard
The cuff inflation line may detach from the endotracheal tube during use. · FDA Class I
Units
430 cases (10 tubes per case)
Sold at
Worldwide Distribution: US (nationwide) AL, AR, AZ, CA, CT, FL, GA, IN, KS, KY, MA, ME, MI, MO, MS, MT, ND, NH, OH, OK, OR, PA, TN, UT, VA, and WV; and countries of: Australia, Canada, Europe (i.e., France, Germany, Great Britain, Ireland, Italy, Netherlands, Portugal, Sweden, & Switzerland), Hong Kong, New Zealand, and United Arab Emirates.
Description
The cuff inflation line may detach from the endotracheal tube during use.
Product
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.5 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.
Manufacturer(s)
Halyard Health
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →