Halyard Health: Medical Device Recall in 2014 - (Recall #: Z-0866-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class I

Date Initiated: November 17, 2014

Date Posted: December 31, 2014

Recall Number: Z-0866-2015

Event ID: 69910

Reason for Recall:

The cuff inflation line may detach from the endotracheal tube during use.

Status: Terminated

Product Quantity: 430 cases (10 tubes per case)

Code Information:

Product Code: 13221, Lot numbers: AA3213, AA3213V01, AA3231, AA3231V01, AA3249, AA3249V02, AA3253, AA3253V01, AA3274, AA3274V03, AA4062, AA4062V02, AA4062V06, AA4097, AA4097V01, AA4097V03, AA4125V01, AA4134V02, AA4140, AA4140V01, AA4142, AA4142V01, AA4146V02, AA4167V03, AA4170 & AA4170V02.

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated