CLASS I Device recall · Reported 7 Aug 2019 · FDA Enforcement Report

Sheridan Endotracheal Tube contained inside Centurion kit recalled

Centurion Medical Products is recalling Sheridan Endotracheal Tube contained inside Centurion kit code TC7855, distributed in Arkansas. The recall was initiated on 7 Jun 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 2018110290

Quantity recalled80 kits

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-1956-2019
FDA event ID: 83202
Recalling firm: Centurion Medical Products, Williamston, MI
Classification: Class I
Status: Terminated
Recall initiated: 7 Jun 2019
FDA classified: 30 Jul 2019
Reported: 7 Aug 2019
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

7 Jun 2019	Recall initiated by company
30 Jul 2019	Classified by FDA	+53 days
7 Aug 2019	Published in enforcement report	+8 days

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

Reason for recall

Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector becoming disconnected from Endotracheal Tube.

Product as listed by the FDA

Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.

Where it was distributed

Distributed to one account in Arkansas.

Arkansas

Questions about this recall

Why was it recalled?

Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector becoming disconnected from Endotracheal Tube.

Which lots are affected?

Lot 2018110290

Where was it sold?

Distributed to one account in Arkansas.

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 26 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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