Reported Jul 24, 2024 · Ongoing

Cascade IOMAX Cortical Module, REF: 190296-200

Cadwell Industries Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Cadwell Industries Inc · 909 N Kellogg St · Kennewick, WA · 99336-7669

Is this the product you have?

  • Cascade IOMAX Cortical Module
  • REF190296-200
Lot codes and dates
  • UDI00840067100653/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
Amount recalled
26 units

Where it was sold

Why it was recalled

Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in unintended electrical stimulation.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:42 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.