Teleflex Medical recalls Hudson RCI Sheridan airway connectors with specific sizes and lot numbers due to reported disconnections. Check your product code and lot numbers to see if affected.
This voluntary recall is due to reported complaints (<0.0025% of all in scope distributed product) indicating that there is an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the Endotracheal tube.
Teleflex Medical is recalling Hudson RCI Sheridan airway connectors that may disconnect from endotracheal tubes. This issue affects specific sizes and lot numbers, which are listed in the recall notice.
The recall is due to reported complaints indicating that certain lots of the 15 mm Sheridan connector may become disconnected from the endotracheal tube during use. This could lead to airway complications if the connection fails.
Healthcare professionals using these connectors for airway management are most at risk. The recall applies to specific product sizes and lot numbers.
Check the product code (e.g., 5-10312 for 6.0 mm) and lot numbers listed in the recall notice. The affected items are used for tracheal tube/airway management.
Identify your product code and lot numbers to determine if they are in the affected list.
Teleflex Medical reports that specific lots of the 15 mm Sheridan connector may become disconnected from the endotracheal tube, leading to airway complications.
Compare your product code and lot numbers with the list provided in the recall notice.
The recall does not specify a remedy, so contact Teleflex Medical directly for guidance.
We’ve drafted a message you can send Teleflex Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1764-2019 — Teleflex Medical Teleflex Medical Hello, I own a Teleflex Medical that is covered by recall Z-1764-2019 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.
