# FDA recall Z-1882-2024

> **Cadwell Industries Inc** · Class II · device recall initiated 2024-04-23.

## Product

Cascade IOMAX Cortical Module, REF: 190296-200

## Reason for recall

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.

## Distribution

Worldwide - US Nationwide distribution in the state of MD and the countries of Mexico, Canada, Malaysia, India, Taiwan, Saudi Arabia, European Union, Switzerland, South Africa, Iraq, United Kingdom.

## Key facts

- **Recall number:** Z-1882-2024
- **Recalling firm:** Cadwell Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-23
- **Report date:** 2024-05-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kennewick, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1882-2024

## Citation

> AI Analytics. FDA recall Z-1882-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1882-2024. Source: US FDA. Licensed CC0.

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