Teleflex Medical recalls Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column

Recall date

April 17, 2014

Source

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

Recall number

Z-0419-2016

FDA classification

Class II

Brand / firm

Teleflex Medical

Sold / distributed

US Distribution to the states of : AL, AZ, CA, GA, IL, KY, LA, MA, MI, MN, NJ, NY, NC, OH, OK, OR, PA, TN, TX and WA.

Why it was recalled

Product is being recalled due to complaints that the inspiratory and expiratory tubes are transposed.

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

What was recalled

Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column