Z-2495-2021 Class II Terminated
FDA device recall Z-2495-2021 was initiated by Ad-Tech Medical Instrument Corporation on August 9, 2021 and is designated Class II. Reason for recall: Incorrect version of labels were used. The recall status is terminated (terminated January 13, 2023). Affected quantity: 10.
Recall Details
- Product Type
- Devices
- Report Date
- September 29, 2021
- Initiation Date
- August 9, 2021
- Termination Date
- January 13, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10
Product Description
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 Pattern
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.
Code Information
Item Code & Lot #: L-DCL-6DIN Lot # 121260; L-DCL-10DIN Lot #'s 124060 and 120340; L-DCL-16BDIN Lot # 120240.