Reported Sep 29, 2021 · Terminated
Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third…
Ad-Tech Medical Instrument Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Ad-Tech Medical Instrument Corporation · 400 W Oakview Pkwy · Oak Creek, WI · 53154-7213
Is this the product you have?
- Ad-Tech Lightweight
- CABRIO Cable - Product UsageDesigned for the purpose of connecting these electrodes to third party monitors/stimulators
- Lot codes and dates
10 of 10 products
Products covered by this recall # Product as published 1 Item Code & Lot #: L-SRL-10DIN Lot #'s 120340, 122140 and 124140 2 L-SRL-10DIN-84 Lot #'s 126270 and 127270 3 L-SRL-12BDIN Lot # 125250 4 L-SRL-16BDINLot #124150 5 L-SRL-20DINLot # 127060 6 L-SRL-32BDIN Lot # 126070 L-SRL-4DIN Lot #'s 123050, 129150 and 120250 7 L-SRL-64BDIN Lot #127270 8 L-SRL-6DINLot #'s 128060 and 120160 9 L-SRL-8DIN Lot #'s 128150 and 124050 10 L-SRL-8DIN-11 Lot # 125170 - Amount recalled
- 69
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Incorrect version of labels were used.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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