---
title: "Cascade IOMAX Cortical Module, REF: 190296-200 — FDA record Z-2349-2024 | Is It on Recall"
description: "Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in uninten"
url: https://isitonrecall.com/recall/fda-device-z-2349-2024-cascade-iomax-cortical-module-ref-190296-200/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Cascade IOMAX Cortical Module, REF: 190296-200 — FDA record Z-2349-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 17, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Cascade IOMAX Cortical Module, REF: 190296-200
- **Reason**: Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in unintended electrical stimulation.
- **Classification**: Class II
- **Recalling firm**: Cadwell Industries Inc
- **Quantity**: 26 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2349-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2349-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI: 00840067100653/Serial Numbers:19029603AA0224001, 19029603AA0224002, 19029603AA0224003, 19029603AA0224004,19029603AA0224005, 19029603AA0224006, 19029603AA0224007, 19029603AA0224008, 19029603AA0224010, 19029603AA0224021, 19029603AA0224027, 19029603AA0324006, 19029603AA0324007, 19029603AA0324008, 19029603AA0324009, 19029603AA0324010, 19029603AA0424001, 19029603AA0424002, 19029603AA0424003, 19029603AA0424006, 19029603AA0424007, 19029603AA0424008, 19029603AA0424009, 19029603AA0424010, 19029603AA0524003, 19029603AA0524004 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: IL CA OUS: Canada, Germany, India, Italy, Mexico, Poland, South Africa, Spain, Taiwan, United Kingdom

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Illinois](https://isitonrecall.com/state/illinois/)

## Dates in the source

- **Report date**: Jul 24, 2024
- **Recall initiation date**: May 17, 2024
- **Center classification date**: Jul 12, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2349-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Cadwell Industries Inc records](https://isitonrecall.com/brand/cadwell-industries-inc/)