Medical device recalls Moderate risk

Teleflex Medical recalls Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier, Rx Only.

Recall date
April 1, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1558-2015
FDA classification
Class II
Brand / firm
Teleflex Medical
Sold / distributed
US Nationwide and Internationally to the countries of: Belgium and Japan

Why it was recalled

Customer complaints were received of power to the unit ceasing and the display going blank.

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

What was recalled

Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier, Rx Only.

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