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.
Read the official notice →- Date
- 2024-07-24
- Country
- United States
- Brand
- Cadwell Industries
- Product
- Cascade IOMAX Cortical Module, REF: 190296-200
- Classification
- Class II
- Units
- US: IL CA OUS: Canada, Germany, India, Italy, Mexico, Poland, South Africa,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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