FDA recall Z-1047-2025

ROi CPS LLC · Class I · device

Product

regard Item Number: 830106006, LD01114F - Newborn Kit containing the component Neo-Tee Resuscitator. Convenience kit to be used in Labor and Delivery.

Reason for recall

There is a potential for the Inline Controller to be using the spring out of specification causing a loss of positive pressure resulting in the Neo-Tee Resuscitator and/or Circuit will not reach the high and low ends of the PIP and PEEP pressure ranges impacting effective ventilation of the patient..

Distribution

Distribution was made to MO. There was no government/military/foreign distribution.

Key facts

Status
Ongoing
Initiation date
2024-12-26
Report date
2025-02-12
Voluntary/Mandated
Voluntary: Firm initiated
Location
Republic, MO, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1047-2025