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Sunset Natural Products Inc.
Sunset Natural Products Inc.: 173 FDA recall reports
Every food recall the FDA has published for Sunset Natural Products Inc.. The fault, and how the agency graded it.
173Reports
0Class I
0Ongoing
2017-01-04Most recent
What the classes mean
The FDA sorts every recall into one of three classes. The class is the whole story. It is also the part people skip.
Class II is the bulk of every list here. That matters. A long list of Class II says something different from one Class I.
By class
By year reported
Checking whether it affects you
The lot or code number is what matters. Not the product name. A recall covers
specific lots. Yours may not be one of them.
Check the code on your package against the report. The FDA keeps the current
list at fda.gov/safety/recalls.
The reports
The text below is quoted from the FDA record word for word.
Colon Therapy, bulk capsules
F-0978-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Colon Therapy, bulk capsules
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 19,455,300
DHEA 25 mg, bulk capsules
F-0994-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- DHEA 25 mg, bulk capsules
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 1,444,900 capsules
Oyster Dietary Supplement (unknown container size)
F-1033-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Oyster Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Liver Energy, 100 capsules per bottle
F-0932-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Liver Energy, 100 capsules per bottle
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 124 Bottles (18,000 capsules)
Arganine & Pine Bark, bulk capsules
F-0976-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Arganine & Pine Bark, bulk capsules
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 1,335,000 capsules
Esclewe Dietary Supplement (unknown container size)
F-1045-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Esclewe Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Chromium Picolinate Dietary Supplement (unknown container size)
F-1022-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Chromium Picolinate Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Sugar Burner Dietary Supplement (unknown container size)
F-1015-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Sugar Burner Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Strev, bulk capsules
F-0987-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Strev, bulk capsules
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 180,000 capsules
Equs Mas, (30 capsules per bottle)
F-0951-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Equs Mas, (30 capsules per bottle)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 1,600 Bottles, (48,000 capsules)
Test Booster, 90 or 60 capsules per bottle
F-0916-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Test Booster, 90 or 60 capsules per bottle
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 5292 Bottles (337,000 capsules)
Project #3, 60 capsules per bottle
F-0913-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Project #3, 60 capsules per bottle
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 1940 Bottles (120,000 capsules)
Argindione, (50,000 capsule bulk)
F-0935-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Argindione, (50,000 capsule bulk)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 50,000 capsules
Project #2, 90 capsules per bottle
F-0912-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Project #2, 90 capsules per bottle
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 1,000 Bottles (90,000 capsules)
Weight Control, 60 capsules per bottle
F-0954-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Weight Control, 60 capsules per bottle
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 2000 Bottles, (35,000 capsules)
Blanc Dietary Supplement (unknown container size)
F-1039-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Blanc Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Gluco + Chond + MSM, Dietary Supplement (unknown container size)
F-1078-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Gluco + Chond + MSM, Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Carni Care, (50,000 capsule bulk)
F-0921-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Carni Care, (50,000 capsule bulk)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 50,000 capsules
Night Stallion, (80,000 capsule bulk)
F-0919-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Night Stallion, (80,000 capsule bulk)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 80,000 Capsules
Extra Mega Prostamax Dietary Supplement (unknown container size)
F-1027-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Extra Mega Prostamax Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Glow Dietary Supplement (unknown container size)
F-1080-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Glow Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Venocell, bulk capsules
F-1003-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Venocell, bulk capsules
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 100,000 capsules
Moinsage, 60 capsules per bottle
F-0962-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Moinsage, 60 capsules per bottle
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- 28,666 Bottles, (1,720,000 capsules)
Bioxtron Dietary Supplement (unknown container size)
F-1024-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Bioxtron Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Magic Memory Dietary Supplement (unknown container size)
F-1012-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Magic Memory Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Yohimbe Dietary Supplement (unknown container size)
F-1017-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Yohimbe Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Tevass 2 Dietary Supplement (unknown container size)
F-1064-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Tevass 2 Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Prostamax Dietary Supplement (unknown container size)
F-1026-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Prostamax Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Super Inmuno Dietary Supplement (unknown container size)
F-1013-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Super Inmuno Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Tevass Dietary Supplement (unknown container size)
F-1042-2017 · Class II · reported 2017-01-04 · Terminated
- Why it was recalled
- 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
- Product
- Tevass Dietary Supplement (unknown container size)
- Where it went
- Products distributed to Florida, Nevada and the Dominican Republic
- How much
- Unknown
Showing the 30 most recent of 173. The rest are searchable at the FDA enforcement report database.
Read these counts with three things in mind
A firm with more recalls usually makes more products. A contract packer runs
hundreds of lines. It will out-recall a company with one product whatever either
does. This is not a safety ranking.
Most recalls here are voluntary. A firm found its own fault and pulled the stock.
That is the system working. It lands in this database looking the same as a recall
the FDA had to push for.
Terminated means the FDA considers the recall finished. It is not a verdict.
It does not mean anyone was harmed.
Source: openFDA enforcement reports, retrieved 2026-08-05. FDA dataset last updated 2026-07-29.
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