CLASS I ONGOING Device recall · Reported 5 Jul 2023 · FDA Enforcement Report

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal recalled

Teleflex is recalling Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, distributed nationwide in the US. The recall was initiated on 25 May 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUDI/DI 4026704319633, Batch Numbers: 18IG06, 18KG44

Quantity recalled190 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1860-2023
FDA event ID: 92373
Recalling firm: Teleflex, Morrisville, NC
Classification: Class I
Status: Ongoing
Recall initiated: 25 May 2023
FDA classified: 29 Jun 2023
Reported: 5 Jul 2023
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

25 May 2023	Recall initiated by company
29 Jun 2023	Classified by FDA	+35 days
5 Jul 2023	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Product as listed by the FDA

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 1700100

Where it was distributed

US Nationwide distribution including Puerto Rico.

Nationwide Puerto Rico

Questions about this recall

Is Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal recalled?

Yes. Teleflex recalled Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal on 25 May 2023. The recall is Class I and its status is Ongoing. Recall number Z-1860-2023.

Why was it recalled?

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Which lots are affected?

UDI/DI 4026704319633, Batch Numbers: 18IG06, 18KG44

Where was it sold?

US Nationwide distribution including Puerto Rico.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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