Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does not properly connect to...

Date: July 9, 2014
Company: Teleflex Medical
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Teleflex Medical directly.

Affected Products

Hudson RCI, Breathing Circuit, Adult, Single Limb w/Heated Wire, [Respiratory Gas Humidifier, (Direct Patient Interface)]. The Hudson Heated Wire Ventilator Circuit is intended as a conduit for respiratory gas between a patient and a ventilator, and includes heated wires for use with a Concha Column Humidifier.

Quantity: 11,679 units

Why Was This Recalled?

The temperature probe does not properly connect to the temperature port.

Where Was This Sold?

This product was distributed to 16 states: CA, FL, KS, KY, MA, MI, MO, NE, NJ, NY, NC, OH, PA, TN, TX, VA

Affected (16 states)Not affected

About Teleflex Medical

Teleflex Medical has 204 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report