Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the Recalled by Ad-Tech Medical Instrument Corporation Due to Incorrect version of labels were used.

Date: August 9, 2021
Company: Ad-Tech Medical Instrument Corporation
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Ad-Tech Medical Instrument Corporation directly.

Affected Products

Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.

Quantity: 69

Why Was This Recalled?

Incorrect version of labels were used.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Ad-Tech Medical Instrument Corporation

Ad-Tech Medical Instrument Corporation has 17 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report