Data Foundry

Medical device recalls 2021

Ad-Tech Lightweight TECH ATTACH Cable — Class II medical device recall Z-2495-2021

Terminated recall by Ad-Tech Medical Instrument Corporation, reported 2021-09-29, distributed nationwide. Incorrect version of labels were used.

Recall numberZ-2495-2021
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAd-Tech Medical Instrument Corporation, Oak Creek, WI, United States
Recall initiated2021-08-09
Classified2021-09-20
Reported by FDA2021-09-29
Terminated2023-01-13
DistributedNationwide (US)
Countries outside the USCA, ES, FR, GB, GR, IT
Quantity10
Reason classeslabeling
Lot numbers120240, 120340, 121260, 124060, L-DCL-10DIN, L-DCL-16BDIN, L-DCL-6DIN

Product

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.

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-2495-2021. 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.