Recalled Teleflex Medical Hudson RCI Sheridan Preformed tubes (3.0-9.0mm) may disconnect from breathing tubes, causing oxygenation issues. Check product references and batch numbers listed in the recall.
Reported complaints indicate an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the endotracheal tube (ETT). Disconnection from the breathing circuit may result in insufficient oxygenation, requiring medical intervention.
Teleflex Medical is recalling specific sizes of Hudson RCI Sheridan Preformed tubes due to reports of them disconnecting from endotracheal tubes. This disconnection could lead to insufficient oxygenation and require medical intervention.
The tubes may disconnect from the endotracheal tube during use, which can cause insufficient oxygenation. This requires medical intervention to address potential breathing difficulties.
Healthcare professionals using these tubes for airway management are most at risk, particularly those handling the recalled sizes and batch numbers listed in the recall.
Check the product reference (REF) numbers and batch numbers listed in the recall. The recalled sizes range from 3.0 mm to 9.0 mm, with specific batch numbers provided for each size.
Identify the product reference (REF) number and batch numbers listed in the recall to confirm if your tube is affected.
Reported complaints indicate an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the endotracheal tube, which may cause insufficient oxygenation.
Check the product reference (REF) number and batch numbers listed in the recall for the specific sizes (3.0 mm to 9.0 mm) provided in the document.
No, but healthcare professionals should check if their tubes are in the recalled list before using them to avoid disconnection risks.
We’ve drafted a message you can send Teleflex Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2314-2019 — Teleflex Medical Teleflex Medical Hello, I own a Teleflex Medical that is covered by recall Z-2314-2019 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.
