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[Recalled] Sheridan/CF Novaplus 7.0 mm, Product Code V5-10114 Product Usage: Tracheal tube/airway management — This voluntary recall is due to reported complaints (<0.0025% of all in scope d… | FDA 2019-05-24

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

ProductSheridan/CF Novaplus 7.0 mm, Product Code V5-10114 Product Usage: Tracheal tube/airway management
Brand / manufacturerTeleflex Medical
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1765-2019
Country of noticeUnited States
Risk levelClass I
Hazard typerecall
Notice date24 May 2019

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: This voluntary recall is due to reported complaints (<0.0025% of all in scope distributed product) indicating that there is an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the Endotracheal tube.

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 Medical

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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