# FDA recall Z-2495-2021

> **Ad-Tech Medical Instrument Corporation** · Class II · device recall initiated 2021-08-09.

## Product

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

## Reason for recall

Incorrect version of labels were used.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of DC, FL, MI, NY, PA and TX and the countries of Spain, France, Italy, Greece, Great Britain and Canada.

## Key facts

- **Recall number:** Z-2495-2021
- **Recalling firm:** Ad-Tech Medical Instrument Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-08-09
- **Report date:** 2021-09-29
- **Termination date:** 2023-01-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Oak Creek, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2495-2021

## Citation

> AI Analytics. FDA recall Z-2495-2021. Retrieved 2026-07-12 from https://api.ai-analytics.org/recall/Z-2495-2021. Source: US FDA. Licensed CC0.

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