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[Recalled] Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170120 — Reports of disconnection of the 15mm connector from the endotracheal tube (ET t… | FDA 2023-05-25

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170120
Brand / manufacturerTELEFLEX LLC
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1837-2023
Country of noticeUnited States
Risk levelClass I
Hazard typerecall
Notice date25 May 2023
EAN / barcode14026704644879

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).

Read the full official notice →

Related recalls from TELEFLEX LLC

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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