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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 72877

10 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
October 05, 2015
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Sunset Natural Products Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

10 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 10

Abee Med, 60 capsules per bottle. Manufactured by Sunset Natural Products

F-0536-2016
Recall number
F-0536-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Quantity
3,149 bottles (240,000 caps)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Code information

Lot # 420415 Exp. Date 04/18 UPC 850993004017

Distribution pattern

FL and NV

food · product 2 of 10

Argindione, sold as bulk of 50,000 capsules.

F-0537-2016
Recall number
F-0537-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Quantity
100,000 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Code information

Lot # 480514 Exp. Date 05/17 and Lot # 320614 Exp. Date 06/17

Distribution pattern

FL and NV

food · product 3 of 10

Chardon de Marie, 60 capsules per bottle. Manufactured by Sunset Natural Products

F-0538-2016
Recall number
F-0538-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Quantity
3,260 bottles (200,000 caps)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Code information

Lot # 141214 Exp. Date 12/17 UPC 897666001157

Distribution pattern

FL and NV

food · product 4 of 10

Moinsage, 60 capsules per bottle. Manufactured by Sunset Natural Products

F-0539-2016
Recall number
F-0539-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Quantity
5,000 bottles (300,000 caps)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Code information

Lot # 030615 Exp. Date 07/18 UPC 897666001164

Distribution pattern

FL and NV

food · product 5 of 10

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

F-0540-2016
Recall number
F-0540-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Quantity
50,000 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Code information

Lot # 110315 Exp. Date 04/18

Distribution pattern

FL and NV

food · product 6 of 10

Prostaliv, 60 capsules per bottle. Manufactured by Sunset Natural Products

F-0541-2016
Recall number
F-0541-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Quantity
5000 bottles (300,000)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Code information

Lot # 180215 Exp Date 02/18 UPC 897666001144,

Distribution pattern

FL and NV

food · product 7 of 10

Prostamax DUO, 60 capsules per bottle. Manufactured by Sunset Natural Products

F-0542-2016
Recall number
F-0542-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Quantity
4,000 bottles (240,000 capsules)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Code information

Lot # 140515 Exp. Date 05/18 UPC 850993004055,

Distribution pattern

FL and NV

food · product 8 of 10

Prostax Forte, sold in bulk of 50,000 capsules.

F-0543-2016
Recall number
F-0543-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Quantity
50,000 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Code information

Lot # 120315 Exp. Date 03/18

Distribution pattern

FL and NV

food · product 9 of 10

Venocell, sold in bulk of 50,000 capsules.

F-0544-2016
Recall number
F-0544-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Quantity
100,000 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Code information

Lot # 160614 Exp. Date 06/17 and Lot # 490914 Exp. Date 10/17

Distribution pattern

FL and NV

food · product 10 of 10

Hepasil, sold in bulk of 500,000 capsules.

F-0617-2016
Recall number
F-0617-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Quantity
500,000 capsules

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Code information

Lot # 080315 Exp. Date 03/18

Distribution pattern

FL and NV