Ad-Tech Medical Instrument Corporation recalls Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party

Recalled September 29, 2021 · FDA recall Z-2494-2021 · Ad-Tech Medical Instrument

Hazard

Incorrect version of labels were used. · FDA Class II

Units

Sold at

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.

Description

Incorrect version of labels were used.

Product

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

Manufacturer(s)

Ad-Tech Medical Instrument Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →