Recall Z-2494-2021— Ad-Tech Medical Instrument Corporation
Class II · Terminated
Class II FDA medical device recall by Ad-Tech Medical Instrument Corporation, initiated 2021-08-09, terminated 2023-01-13. FDA's recall record names no specific 510(k) clearance for this event. Product: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.. Reason: Incorrect version of labels were used..
- Recalling firm
- Ad-Tech Medical Instrument Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-08-09
- Terminated
- 2023-01-13
- Firm location
- Oak Creek, WI, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.