PlainRecalls
FDA Devices Critical Class I Ongoing

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382065

Reported: July 5, 2023 Initiated: May 25, 2023 #Z-1939-2023

Product Description

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382065

Reason for Recall

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

Details

Recalling Firm
TELEFLEX LLC
Units Affected
2140 units
Distribution
US Nationwide distribution including Puerto Rico.
Location
Morrisville, NC

Frequently Asked Questions

What product was recalled?
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382065. Recalled by TELEFLEX LLC. Units affected: 2140 units.
Why was this product recalled?
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 5, 2023. Severity: Critical. Recall number: Z-1939-2023.