FDA recall Z-1765-2019

Product

Sheridan/CF Novaplus 7.0 mm, Product Code V5-10114 Product Usage: Tracheal tube/airway management

Reason for recall

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.

Distribution

Worldwide - US Nationwide Distribution

Key facts

Status

Terminated

Initiation date

2019-05-24

Report date

2019-06-26

Termination date

2022-02-15

Voluntary/Mandated

Voluntary: Firm initiated

Location

Morrisville, NC, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1765-2019