Cadwell Industries Inc FDA Recalls

2 recalls on file across devices, 0 of them Class I and 2 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
Cascade IOMAX Cortical Module, REF: 190296-200Class IIMay 17, 2024Electroneurodiagnostic medical device may contain a defecti	Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to	Class IIDevices	May 17, 2024
Cascade IOMAX Cortical Module, REF: 190296-200Class IIApr 23, 2024There is the potential that an electroneurodiagnostic medica	There is the potential that an electroneurodiagnostic medical device insulator may be installed incorrectly wh	Class IIDevices	Apr 23, 2024