Cadwell Industries Inc 2024-07-24 Health serious FDA
Health · FDA · Recall #FDA-Z-2349-2024
Cascade IOMAX Cortical Module, REF: 190296-200 Recall
Issued July 24, 2024 · Cadwell Industries Inc
In July 2024, Cadwell Industries Inc recalled the Cascade IOMAX Cortical Module, REF: 190296-200, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in unintended electrical stimulation.
What you should do
- 1 Stop using Cascade IOMAX Cortical Module, REF: 190296-200 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Cadwell Industries Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Cadwell Industries Inc
- Category
- Health
- Recall date
- July 24, 2024
- Units affected
- Not reported
- Sold at
- US: IL CA OUS: Canada, Germany, India, Italy, Mexico, Poland, South Africa, Spain, Taiwan, United Kingdom
- Recall number
- FDA-Z-2349-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Cadwell Industries Inc has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.