Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Ongoing Initiated Feb 23, 2023 (4 years ago)

NaturalCare bioAllers

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

Cause type: Failed specification

A physical or chemical test other than potency, dissolution, impurity or stability failed - pH, viscosity, appearance, tablet integrity, fill volume. A product outside its own specification may not perform as designed, even if the active ingredient is present. All failed specification recalls.

What was recalled

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

Drug: Alcohol

Recalling firm
Nutraceutical Corporation
Origin
UT, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0439-2023 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.

Other Alcohol recalls

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Other recalls by Nutraceutical Corporation

All 2023 recalls
Class II · Moderate risk

NaturalCare

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

Ongoing Failed specification Nutraceutical Corporation D-0440-2023
Class II · Moderate risk

NatraBio

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

Ongoing Failed specification Nutraceutical Corporation D-0438-2023
Class II · Moderate risk

NaturalCare bioAllers

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

Ongoing Failed specification Nutraceutical Corporation D-0437-2023