Teleflex Medical recalls Hudson RCI One Way Valve (REF 1644) due to potential disconnection causing ventilation interruption. Affected units sold in respiratory/anesthesia circuits.
These one-way valves may disconnect at the joint between the two components that make up the device, which would cause an interruption of ventilation to the patient.
Teleflex Medical is recalling Hudson RCI One Way Valves with capped monitoring port (REF 1644) because they may disconnect at the joint, interrupting patient ventilation. This could lead to serious breathing issues during medical procedures.
The one-way valve may disconnect at the joint between components, causing an interruption in the patient's ventilation. This could lead to breathing difficulties or other complications during medical procedures.
Healthcare professionals using these valves in respiratory and anesthesia equipment. Patients undergoing procedures with this valve could be at risk if disconnection occurs.
Check for the model number REF 1644 on the valve. These valves were sold in respiratory and anesthesia circuits. Lot numbers include 74D1501706 through 74H1702374.
Inspect the valve for signs of disconnection at the joint between components.
Reach out to Teleflex Medical for guidance on replacement or repair options.
The one-way valve may disconnect at the joint between components, causing an interruption in patient ventilation during medical procedures.
The affected model is REF 1644.
Check for the model number REF 1644 and lot numbers listed in the recall notice (74D1501706 through 74H1702374).
We’ve drafted a message you can send Teleflex Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1403-2018 — Teleflex Medical Teleflex Medical Hello, I own a Teleflex Medical that is covered by recall Z-1403-2018 from Teleflex Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
