Teleflex recalls Slick Set Cuffed Endotracheal Tubes with 15mm connector that may disconnect during use. Affected products include specific batch numbers and model references. Consumers should check their items and contact Teleflex for details.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling certain Slick Set Cuffed Endotracheal Tubes and Stylet Sets due to reports of the 15mm connector disconnecting from the tube. This could lead to breathing difficulties if the tube becomes dislodged during medical procedures.
The 15mm connector on the endotracheal tube can become disconnected during medical procedures. This disconnection could cause the tube to become unplugged, potentially leading to breathing difficulties for patients.
Healthcare professionals using these tubes for intubation procedures are most at risk. Patients receiving intubation care with the affected products may experience breathing issues if the tube disconnects.
Check for the product name 'Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal' with reference number REF 170075. Affected items have specific batch numbers listed in the recall notice.
Identify the product by checking the reference number REF 170075 and batch numbers listed in the recall notice.
Reach out to Teleflex for further assistance or to confirm if your product is affected.
Teleflex is recalling these products due to reports of the 15mm connector disconnecting from the endotracheal tube during use.
Check for the reference number REF 170075 and specific batch numbers listed in the recall notice.
Contact Teleflex directly to determine if your product is affected and for further instructions.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1832-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1832-2023 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.
