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RECALLING FIRM / COMPANY

Sundial Herbal Products Recalls

Are there any recent recalls involving Sundial Herbal Products?

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.

68 FDA product recordsLatest initiation: Jun 30, 2020

Same product name.
Different batch.
Check the label.

All recall records involving Sundial Herbal Products

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

68 recall recordsPage 5 of 6
Class II
FDA status: Terminated

"Sundial***Traditional Jamaican***ORGANIC***Original Maroon Recipe***WOOD AND ROOT TONIC***used for centuries in…

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →
Class II
FDA status: Terminated

"SUNDIAL***KOROMANTEE***Colonic & Intestinal Cleaner***used by the descendants of the Koromantee people in Jamaica to…

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →
Class II
FDA status: Terminated

"***Sundial***ASHANTI**WEIGHT LOSS ENERGY LIFTER and APPETITE SUPPRESSER***" packaged in glass bottles

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →
Class II
FDA status: Terminated

"SUNDIAL***TRADITIONAL AFRICAN MANBACK TONIC***remember the strength of the reproductive organ, reflects the strength…

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →
Class II
FDA status: Terminated

"SUNDIAL***TRADITIONAL HERBAL FORMULA***DIABETICS***" packaged in boxes

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →
Class II
FDA status: Terminated

"SUNDIAL***TRADITIONAL HERBAL FORMULA***ASTHMA***" packaged in boxes

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →
Class II
FDA status: Terminated

"SUNDIAL***TRADITIONAL HERBAL FORMULA***BLOOD PRESSURE***" packaged in boxes

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →
Class II
FDA status: Terminated

"SUNDIAL***TRADITIONAL HERBAL FORMULA***HEART***" packaged in boxes

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →
Class II
FDA status: Terminated

"SUNDIAL***TRADITIONAL HERBAL FORMULA***Worms & Parasites***" packaged in boxes

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →
Class II
FDA status: Terminated

"SUNDIAL***TRADITIONAL HERBAL FORMULA***Flu-Allergies HayFever***" packaged in boxes

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →
Class II
FDA status: Terminated

"SUNDIAL***TRADITIONAL HERBAL FORMULA***ARTHRITIS***" packaged in boxes

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →
Class II
FDA status: Terminated

"AXUM ETHOIPIAN HONEY BEVERAGE***SUNDIAL HERBS***"

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

Labeling / mislabelingView details →

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Same product name. Different batch. Details matter.

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