NDDd Medical Technologies, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0596-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

EasyOne Pro Respiratory Analysis System Pulmonary Function Testing Device, Model 3000-1

Product Classification:

Class II

Date Initiated: August 15, 2017

Date Posted: December 11, 2019

Recall Number: Z-0596-2020

Event ID: 83992

Reason for Recall:

The CO/CO2 sensor cable harness may have lower electromagnetic shielding, which might have resulted in a non-compliance with the IEC 60601-1-2 standard. As a consequence of a lower electromagnetic shielding provided by the cable harness, the CO/CO2 sensor could have been influenced by high frequencies emitted by very close devices.

Status: Terminated

Product Quantity: 37 total devices

Code Information:

Serial Numbers: 550066 550067 550068 550069 550071 550072

Distribution Pattern:

The products were distributed to the following US states: KY, MO, NY, OH, PA

Voluntary or Mandated:

Voluntary: Firm initiated