Cadwell Industries recalls

2 official recalls and safety alerts involving Cadwell Industries since 2024-05, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Cadwell Industries or the relevant agency.

1. 2024-07-24
2. US
   Drugs & medicalClass II

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

   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 · DeviceCadwell Industries IncUS: IL CA OUS: Canada, Germany, India, Italy, Mexico, Poland, South Africa,…Official notice →
3. 2024-05-29
4. US
   Drugs & medicalClass II

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

   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.

   FDA · DeviceCadwell Industries IncWorldwide - US Nationwide distribution in the state of MD and the countries of…Official notice →