Teleflex recalls Slick Set Cuffed Endotracheal Tubes with reported disconnection risks. 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 during medical procedures if the tube becomes disconnected.
The 15mm connector on the endotracheal tube can disconnect during use, potentially causing breathing difficulties for patients. This disconnection risk occurs even with normal handling and use in medical settings.
Healthcare professionals using the affected endotracheal tubes for patient intubation are most at risk. Patients receiving intubation care with these specific products may also be affected.
Check for the model reference REF 170055 and batch numbers listed in the recall notice. Affected products include specific batch codes like 18FG18, 18GG14, and others as detailed in the recall.
Identify the model reference and batch numbers listed in the recall notice to confirm if your product is affected.
The recall reports disconnections that could cause breathing difficulties during medical procedures, but the hazard is not described as causing serious injury in normal use.
Check for the model reference REF 170055 and batch numbers listed in the recall notice, such as 18FG18, 18GG14, and others.
The recall does not specify a remedy, so contact Teleflex directly 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-1828-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1828-2023 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.
