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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 8 of 15
Class II
FDA status: Terminated

Venocell, bulk 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

Shilaji 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

Triphala 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

Shatavari 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

Ashwaganda 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

Bio Moringa 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

Liver Clean 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

Body Shape 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

Prostate Plus 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

Magic Memory 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

Super Inmuno 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

Nutriplex 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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Same product name. Different batch. Details matter.

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