Ad-Tech Lightweight TECH ATTACH Cable Recall: Incorrect Labels Cause Safety Risk
Ad-Tech recalls lightweight cables with incorrect labels that could lead to improper connections. Affected items have specific lot numbers. Contact Ad-Tech for details.
Lower-risk recall
Incorrect version of labels were used.
Contact the company
What happened, in plain English
Ad-Tech is recalling lightweight cables that have incorrect labels. This could lead to improper connections with medical monitors or stimulators, potentially causing safety issues. Read more at govinfonow.com/recall/62007-ad-tech-lightweight-tech-attach-cable-recall-incorrect-labels-cause.
Source Summary by GovInfoNow · govinfonow.com/recall/62007-ad-tech-lightweight-tech-attach-cable-recall-incorrect-labels-cause · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2495-2021
Cite this page
“Ad-Tech Lightweight TECH ATTACH Cable Recall: Incorrect Labels Cause Safety Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62007-ad-tech-lightweight-tech-attach-cable-recall-incorrect-labels-cause. Based on FDA recall #Z-2495-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2495-2021%22&limit=1).
Why it’s dangerous
Incorrect labels on the cables could lead to improper connections with medical monitors or stimulators. This might cause incorrect readings or malfunctioning equipment during medical procedures.
Who’s affected
Medical professionals using these cables for patient monitoring or stimulation are most at risk. The recall affects specific lot numbers of the lightweight cables.
How to tell if you have this one
Check for lot numbers: L-DCL-6DIN Lot #121260, L-DCL-1:0DIN Lot #s 124060 and 120340, L-DCL-16BDIN Lot #120240. The cables are designed for connecting electrodes to third-party medical devices.
- Brand
Ad-Tech- Category
Medical device
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- 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.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-2494-2021 | Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.; Item Code & Lot #: L-SRL-10DIN Lot #'s 120340, 122140 and 124140; L-SRL-10DIN-84 Lot #'s 126270 and 127270; L-SRL-12BDIN Lot # 125250; L-SRL-16BDINLot #124150; L-SRL-20DINLot # 127060; L-SRL-32BDIN Lot # 126070 L-SRL-4DIN Lot #'s 123050, 129150 and 120250; L-SRL-64BDIN Lot #127270; L-SRL-6DINLot #'s 128060 and 120160; L-SRL-8DIN Lot #'s 128150 and 124050; L-SRL-8DIN-11 Lot # 125170 | 69 |
| Z-2495-2021 | Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.; Item Code & Lot #: L-DCL-6DIN Lot # 121260; L-DCL-10DIN Lot #'s 124060 and 120340; L-DCL-16BDIN Lot # 120240. | 10 |
| Z-2496-2021 | Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.; Item Code & Lot #: L-DC-10DIN Lot #'s 121240 and 126270. | 8 |
What to do — step by step
Check Product Labels
Look for the specific lot numbers listed in the recall notice to determine if your cable is affected.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 5 states.
FDA 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.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: District of Columbia, Florida, Michigan, New York, Pennsylvania, Texas.
Recall timeline
FDA terminated this recall 17 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2495-2021 (August 9, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2495-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.