Ad-Tech Lightweight CABRIO Cable — Class II medical device recall Z-2494-2021
Terminated recall by Ad-Tech Medical Instrument Corporation, reported 2021-09-29, distributed nationwide. Incorrect version of labels were used.
| Recall number | Z-2494-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ad-Tech Medical Instrument Corporation, Oak Creek, WI, United States |
| Recall initiated | 2021-08-09 |
| Classified | 2021-09-20 |
| Reported by FDA | 2021-09-29 |
| Terminated | 2023-01-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, ES, FR, GB, GR, IT |
| Quantity | 69 |
| Reason classes | labeling |
| Lot numbers | 120160, 120250, 120340, 122140, 123050, 124050, 124140, 124150, 125170, 125250, 126070, 126270, 127060, 127270, 128060, 128150, 129150, L-SRL-10DIN, L-SRL-10DIN-84, L-SRL-12BDIN, L-SRL-16BDINLOT, L-SRL-20DINLOT, L-SRL-32BDIN, L-SRL-4DIN, L-SRL-64BDIN, L-SRL-6DINLOT, L-SRL-8DIN, L-SRL-8DIN-11 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2494-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.