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RECALLING FIRM / COMPANY

Sunset Natural Products Inc. Recalls

Are there any recent recalls involving Sunset Natural Products Inc.?

0 recall records initiated in the snapshot’s last 365 days. 0 are FDA-listed ongoing with no termination date.FDA data updated September 16, 2026 · Snapshot assessed September 18, 2026

The FDA identifies this company as the recalling firm; this does not establish that it is the manufacturer, retailer or brand owner. “Recent ongoing” means initiated within 365 days of September 18, 2026, FDA status “Ongoing,” and no termination date. This snapshot cannot confirm what is active today.

173 FDA product recordsLatest initiation: Oct 13, 2015

Same product name.
Different batch.
Check the label.

All recall records involving Sunset Natural Products Inc.

Initiated in 2015. Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

173 recall recordsPage 14 of 15
Class II
FDA status: Terminated

Insulow Dietary Supplement (unknown container size)

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Class II
FDA status: Terminated

First Defense Probiotic Dietary Supplement (unknown container size)

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Class II
FDA status: Terminated

Triflex Dietary Supplement (unknown container size)

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Class II
FDA status: Terminated

Gluco + Chond + MSM, Dietary Supplement (unknown container size)

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Class II
FDA status: Terminated

De Pura Fibra Dietary Supplement (unknown container size)

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Class II
FDA status: Terminated

Glow Dietary Supplement (unknown container size)

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Class II
FDA status: Terminated

Diet III Dietary Supplement (unknown container size)

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Class II
FDA status: Terminated

Abee Med, 60 capsules per bottle.

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Class II
FDA status: Terminated

Argindione, sold as bulk of 50,000 capsules.

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Class II
FDA status: Terminated

Chardon de Marie, 60 capsules per bottle.

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Class II
FDA status: Terminated

Moinsage, 60 capsules per bottle.

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Class II
FDA status: Terminated

Neuro-Cetin, sold in bulk 50,000 capsules.

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall…

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Same product name. Different batch. Details matter.

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