Nihon Kohden America Inc: Medical Device Recalls in 2021

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Nihon Kohden America Inc in 2021. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

WMTS Telemetry Receiver, Multiple Patient Receiver, Model Number/ UDI: ORG 9100A/ 00841983102554 ORG 9110A/ 00841983102561 ORG 9700A/No UDI
PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No. 01454 RoHS Compliant; PSG-100 Head Box; UDI (01) 04931921108383; Made in Japan The PSG-1100 Sleep Diagnostic System is a digital PSG amplifier intended to record the electrical activity of the brain (EEG) and other bio-potential signals and to record physiological data required for sleep studies.