FDA recall Z-1875-2023

Product

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035

Reason for recall

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

Distribution

US Nationwide distribution including Puerto Rico.

Key facts

Status

Ongoing

Initiation date

2023-05-25

Report date

2023-07-05

Voluntary/Mandated

Voluntary: Firm initiated

Location

Morrisville, NC, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1875-2023