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[Recalled] Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators. — Incorrect version of labels were used | FDA 2021-08-09

recall fda device united-states

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

ProductAd-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Brand / manufacturerAd-Tech Medical Instrument Corporation
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2494-2021
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date09 August 2021

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Incorrect version of labels were used.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Ad-Tech Medical Instrument Corporation

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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