Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Reported: September 29, 2021 Initiated: August 9, 2021 #Z-2494-2021
Product Description
Ad-Tech Lightweight CABRIO 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.
Details
- Recalling Firm
- Ad-Tech Medical Instrument Corporation
- Units Affected
- 69
- 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.
- Location
- Oak Creek, WI
Frequently Asked Questions
What product was recalled? ▼
Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.. Recalled by Ad-Tech Medical Instrument Corporation. Units affected: 69.
Why was this product recalled? ▼
Incorrect version of labels were used.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 29, 2021. Severity: Moderate. Recall number: Z-2494-2021.
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