FDA recall Z-1782-2018

Ondamed Inc · Class II · device

Product

Ondamed Biofeedback Device, Model No. 001-00-0101 The product is a battery powered biofeedback device that is indicated for relaxation training and muscle re-education and prescription use.

Reason for recall

The firm was marketing the Ondamed System in the US without marketing clearance. As a corrective action, the firm revised its device design to comply with regulations. The firm has notified customers that an upgrade for the device is now available, which includes the addition of direct readout and audio signals for heart rate, and visual patient readout of blood oxygen content SpO2.

Distribution

Worldwide Distribution - USA (nationwide) and to the counties of : Canada and Taiwan.

Key facts

Status
Terminated
Initiation date
2017-07-07
Report date
2018-05-16
Termination date
2020-04-24
Voluntary/Mandated
Voluntary: Firm initiated
Location
New Windsor, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1782-2018