Sunset Natural Products Recalls Nova Life Dietary Supplement Under Consent Decree
Sunset Natural Products Inc. is recalling Nova Life Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class II, which corresponds to a severity score of 4 (Severe) per the rubric, as it involves a reasonable probability of temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Plain-English summary
Sunset Natural Products Inc. is recalling Nova Life Dietary Supplement (unknown container size) pursuant to a consent decree. The decree prohibits the company and its owners from marketing dietary supplements until they recall and destroy all dietary supplements manufactured, prepared, processed, packed, labeled, held, and/or distributed between April 2, 2014, and the date of the decree's entry on September 25, 2015.
The recall is conducted under FDA supervision in accordance with the procedures provided in the consent decree. Known lot number 270715 is included in the recall. The products were distributed to Florida, Nevada, and the Dominican Republic.
Consumers who have purchased Nova Life Dietary Supplement should stop using the product and follow the instructions provided by the recalling firm or the FDA for disposal or return.
The recalled product
- Product
- Nova Life Dietary Supplement (unknown container size)
- Manufacturer
- Sunset Natural Products Inc.
- Category
- Food — Dietary Supplement
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (11)
- As persuant to the Consent Decree
- the firm agreed to "recall and destroy
- under FDA's supervision
- in accordance with the procedures provided in paragraph 6
- ALL dietary supplements that were manufactured
- prepared
- processed
- packed
- labeled
- held and/or distributed between April 2
- 2015. Known lot: Lot # 270715
Distribution
Part of a larger recall action
This product is one of 163 recalled by Sunset Natural Products Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 163 products in this recall →Related recalls
Same manufacturer · Sunset Natural Products Inc.
See all →- SevereSunset Natural Products Recalls Equs Dietary Supplement Under Consent Decree
FDA (Food) · 2017-01-04
- SevereSunset Natural Products Recalls Prostate Plus Dietary Supplement
FDA (Food) · 2017-01-04
- SevereSunset Natural Products Recalls Kelp Acerola and Green Tea Capsules
FDA (Food) · 2017-01-04
- SevereSunset Natural Products Recalls Jagra Dietary Supplement Under Consent Decree
FDA (Food) · 2017-01-04
- SevereSunset Natural Products Recalls Collagen Hydrolyzed Dietary Supplements
FDA (Food) · 2017-01-04
Same hazard · mis labeling
See all →- SevereImperio Distribution Recalls Beef Jerky Produced Without Federal Inspection
USDA FSIS · 2026-10-24
- HighJ K Patisserie Chocolate Chip Cookies Recalled for Undeclared Soy
FDA (Food) · 2026-10-14
- HighFreshPoint Recalls Cranberry Chicken Salad Wedges for Undeclared Egg Allergen
FDA (Food) · 2026-10-14
- HighJ K Patisserie & Bakery LLC Recalls Croissants for Undeclared Egg
FDA (Food) · 2026-10-14
- LowMindray ePM Series Patient Monitor Manuals Recalled for Alarm Clarification
FDA (Devices) · 2026-10-14
Similar recalls
- SevereSunset Natural Products Recalls Venocell Dietary Supplement Under Consent Decree
FDA (Food) · 2016-02-24
- ModerateSunset Natural Products Recalls Prostaliv Dietary Supplement Under Consent Decree
FDA (Food) · 2016-02-24
- ModerateSunset Natural Products Recalls Moinsage Dietary Supplement Capsules
FDA (Food) · 2016-02-24
- ModerateSunset Natural Products Recalls Neuro-Cetin Dietary Supplement Capsules
FDA (Food) · 2016-02-24
- ModerateSunset Natural Products Recalls Prostax Forte Dietary Supplement
FDA (Food) · 2016-02-24
- ModerateSunset Natural Products Recalls Hepasil Dietary Supplement Capsules
FDA (Food) · 2016-02-24