CLASS II ONGOING Drug recall · Reported 17 Sep 2025 · FDA Enforcement Report

Neuroquell & Neuroquell Plus recalled by Atlantic Management Resources

Atlantic Management Resources is recalling Neuroquell & Neuroquell Plus. The recall was initiated on 27 Aug 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # B-02 Batch #: 1087920520 Product # R937 BBE#31-05-21( May 31, 2021) Batch # 1087920920 Product # R937 BBE# 31-05-21 (May 31, 2021)
Quantity recalled72 containers

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0629-2025
FDA event ID
97345
Recalling firm
Atlantic Management Resources, Westborough, MA
Classification
Class II
Status
Ongoing
Recall initiated
27 Aug 2025
FDA classified
10 Sep 2025
Reported
17 Sep 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail

Timeline

27 Aug 2025Recall initiated by company
10 Sep 2025Classified by FDA+14 days
17 Sep 2025Published in enforcement report+7 days

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

Reason for recall

cGMP violations

Product as listed by the FDA

Neuroquell & Neuroquell Plus, .22 fl. Oz (6.6mL),Mfg. For/Dist. By Claire Ellen Products, P.O. Box 901 Westboro, MA 01581 USA, NDC 66233712-01

Where it was distributed

Product was distributed via the internet.

Stores named: Online Retailers

Questions about this recall

Is Neuroquell & Neuroquell Plus recalled?

Yes. Atlantic Management Resources recalled Neuroquell & Neuroquell Plus on 27 Aug 2025. The recall is Class II and its status is Ongoing. Recall number D-0629-2025.

Why was it recalled?

cGMP violations

Which lots are affected?

Lot # B-02 Batch #: 1087920520 Product # R937 BBE#31-05-21( May 31, 2021) Batch # 1087920920 Product # R937 BBE# 31-05-21 (May 31, 2021)

Where was it sold?

Product was distributed via the internet.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

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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