Teleflex recalls Slick Set Cuffed Endotracheal Tubes with specific batch numbers due to reported connector disconnections. Affected products may disconnect during use, posing a risk of airway obstruction.
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 because reports indicate the 15mm connector can disconnect from the tube. This disconnection could lead to airway obstruction if the tube becomes disconnected during medical procedures.
The 15mm connector on the endotracheal tube can become disconnected during use, which may cause the tube to become dislodged from the patient's airway. This disconnection could lead to airway obstruction and potential respiratory distress if not addressed immediately.
Healthcare professionals using the affected endotracheal tubes during medical procedures are most at risk. Patients receiving intubation care with these specific products could face airway obstruction if the tube disconnects.
Check for the product name 'Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal' with the specific batch numbers listed: 19HT48, 19KT17, 20AT53, 20BT37, KME22E2493, KME22F1387, KME22H0342. The UDI/DI number 4026704319626 is also associated with these products.
Inspect the 15mm connector on the endotracheal tube for signs of disconnection or damage.
Teleflex is recalling these products due to reports of the 15mm connector disconnecting from the endotracheal tube during use, which could lead to airway obstruction.
The affected batch numbers are 19HT48, 19KT17, 20AT53, 20BT37, KME22E2493, KME22F1387, and KME22H0342.
Look for the product name 'Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal' with the UDI/DI number 4026704319626 and the listed batch numbers.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1836-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1836-2023 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.
