Teleflex recalls Flexi-Set Cuffed Endotracheal Tubes with reported disconnections. Affected products include specific batch numbers and model references. Consumers should check their items against the list provided in the recall notice.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling certain Flexi-Set Cuffed Endotracheal Tubes and Stylet Sets due to reports of the 15mm connector disconnecting from the tube. This could lead to breathing issues if the tube becomes dislodged during medical procedures.
The 15mm connector on the endotracheal tube may disconnect during use, potentially causing breathing difficulties for patients. This disconnection is reported in medical settings but does not typically cause serious injury in normal use.
Healthcare professionals and medical facilities using the affected Flexi-Set products. Those most at risk are individuals handling the tubes during patient care where disconnection could occur.
Check for the product name 'Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal' with the reference number REF 504585. Affected items have specific batch numbers listed in the recall notice.
Identify the product by checking the reference number REF 504585 and batch numbers listed in the recall notice.
This product is for medical use only and is not intended for home use. The recall applies to healthcare settings where disconnection could occur.
Check the product's reference number REF 504585 and batch numbers listed in the recall notice to see if it matches the affected items.
The recall does not specify a remedy, so contact Teleflex directly for guidance on handling the product.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1852-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1852-2023 from Teleflex. 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.
