Cadwell Industries Inc recalls Cascade IOMAX Cortical Module, REF: 190296-200

Recalled July 24, 2024 · FDA recall Z-2349-2024 · Cadwell Industries

Hazard

Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in unintended electrical stimulation. · FDA Class II

Units

26 units

Sold at

US: IL CA OUS: Canada, Germany, India, Italy, Mexico, Poland, South Africa, Spain, Taiwan, United Kingdom

Description

Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in unintended electrical stimulation.

Product

Cascade IOMAX Cortical Module, REF: 190296-200

Manufacturer(s)

Cadwell Industries Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →