CLASS II ONGOING Drug recall · Reported 15 Mar 2023 · FDA Enforcement Report

NaturalCare bioAllers, Mold, Yeast and Dust, Homeopathic recalled

Nutraceutical is recalling NaturalCare bioAllers, Mold, Yeast and Dust, Homeopathic, Liquid Drops, 20% Alcohol(, distributed nationwide in the US. The recall was initiated on 23 Feb 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 222076, Exp: 03/27;
Quantity recalled8,146

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-0439-2023
FDA event ID
91708
Recalling firm
Nutraceutical, Park City, UT
Classification
Class II
Status
Ongoing
Recall initiated
23 Feb 2023
FDA classified
7 Mar 2023
Reported
15 Mar 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

23 Feb 2023Recall initiated by company
7 Mar 2023Classified by FDA+12 days
15 Mar 2023Published in enforcement report+8 days

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

Reason for recall

CGMP Deviations: Raw material recalled by repackager, due to discoloration.

Product as listed by the FDA

NaturalCare bioAllers, Mold, Yeast and Dust, Homeopathic, Liquid Drops, 20% Alcohol, 1 FL OZ( 30mL), Mfd. for Nutraceutical Corp. NaturalCare Park City, UT, 84098 USA

Where it was distributed

Nationwide in the USA.

Nationwide

Questions about this recall

Why was it recalled?

CGMP Deviations: Raw material recalled by repackager, due to discoloration.

Which lots are affected?

Lot 222076, Exp: 03/27;

Where was it sold?

Nationwide in the USA.

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

Other products in this recall event

3 other products · FDA event 91708

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