CLASS II Device recall · Reported 29 Sep 2021 · FDA Enforcement Report

Ad-Tech Tech Attach Cable recalled by Ad-Tech Medical Instrument

Ad-Tech Medical Instrument is recalling Ad-Tech Tech Attach Cable, distributed nationwide in the US. The recall was initiated on 9 Aug 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesItem Code & Lot #: L-DC-10DIN Lot #'s 121240 and 126270.

Quantity recalled8

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2496-2021
FDA event ID: 88590
Recalling firm: Ad-Tech Medical Instrument, Oak Creek, WI
Classification: Class II
Status: Terminated
Recall initiated: 9 Aug 2021
FDA classified: 20 Sep 2021
Reported: 29 Sep 2021
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Other Reasons
Device type: Patient Monitors

Timeline

9 Aug 2021	Recall initiated by company
20 Sep 2021	Classified by FDA	+42 days
29 Sep 2021	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Incorrect version of labels were used.

Product as listed by the FDA

Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.

Where it was distributed

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.

Nationwide District of Columbia Florida Michigan New York Pennsylvania Texas

Questions about this recall

Is Ad-Tech Tech Attach Cable recalled?

Yes. Ad-Tech Medical Instrument recalled Ad-Tech Tech Attach Cable on 9 Aug 2021. The recall is Class II and its status is Terminated. Recall number Z-2496-2021.

Why was it recalled?

Incorrect version of labels were used.

Which lots are affected?

Item Code & Lot #: L-DC-10DIN Lot #'s 121240 and 126270.

Where was it sold?

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.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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