Cadwell Industries recalls Cascade IOMAX Cortical Module (REF: 190296-200) due to potential defective circuit board causing unintended electrical stimulation. Affected units have specific serial numbers.
Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in unintended electrical stimulation.
Cadwell Industries is recalling its Cascade IOMAX Cortical Module (REF: 190296-200) because it may contain a defective printed circuit board that could cause unintended electrical stimulation. This device is used in medical settings for electrophysiological testing, so the risk could affect patient safety during procedures.
The device may contain a defective printed circuit board that can damage other internal components. This defect might lead to unintended electrical stimulation, which could pose a risk during medical procedures.
Medical professionals using the Cascade IOMAX Cortical Module for electrophysiological testing are most at risk. Patients undergoing procedures with this device could be affected if the defect causes unintended electrical stimulation.
Check for the model 'Cascade IOMAX Cortical Module' with serial numbers listed in the recall notice: 19029603AA0224001 through 19029603AA0524004. The product was sold with reference number REF: 190296-200.
Look for the specific serial numbers listed in the recall notice: 19029603AA0224001 through 19029603AA0524004.
The recall indicates a potential risk of unintended electrical stimulation, so it is not safe to use without checking if it is recalled.
The recall does not specify a remedy, so contact Cadwell Industries for further instructions.
Check if your device has the serial numbers listed: 19029603AA0224001 through 19029603AA0524004.
We’ve drafted a message you can send Cadwell to request your refund or repair — edit it as you like.
Subject: Recall Z-2349-2024 — Cadwell Cadwell Hello, I own a Cadwell that is covered by recall Z-2349-2024 from Cadwell. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
