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Cadwell Industries Recalls
2 recalls on record · May 29, 2024 to July 24, 2024 · Medical Devices
July 24, 2024Medical DevicesFDA
Cadwell Industries Inc recalls Cascade IOMAX Cortical Module, REF: 190296-200
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.
May 29, 2024Medical DevicesFDA
Cadwell Industries Inc recalls Cascade IOMAX Cortical Module, REF: 190296-200
Hazard: There is the potential that an electroneurodiagnostic medical device insulator may be installed incorrectly which could result in arcing to patient connections resulting in potential unintended shock to the patient.