Check the Batch

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 3 of 15
Class II
FDA status: Terminated

Artrosamin, 250,000 capsules per bulk order

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

OtherView details →
Class II
FDA status: Terminated

Hepasil, (various bulk amounts)

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

OtherView details →
Class II
FDA status: Terminated

Argindione, (50,000 capsule bulk)

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

OtherView details →
Class II
FDA status: Terminated

Dygeszyme, (50,000 capsule bulk)

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

OtherView details →
Class II
FDA status: Terminated

Prostax Forte, (50,000 capsule bulk)

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

OtherView details →
Class II
FDA status: Terminated

Magnumn, (30 per bottle)

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

OtherView details →
Class II
FDA status: Terminated

Magnun Plus, (30 per bottle)

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

OtherView details →
Class II
FDA status: Terminated

Equs, (30 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…

OtherView details →
Class II
FDA status: Terminated

Equs Mas, (30 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…

OtherView details →
Class II
FDA status: Terminated

Lebytol, 30 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…

OtherView details →
Class II
FDA status: Terminated

ABS Reducer, 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…

OtherView details →
Class II
FDA status: Terminated

Weight Control, 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…

OtherView details →

Found your product? Now check the codes.

Same product name. Different batch. Details matter.

→