Sunset Natural Products Recalls Thor Dietary Supplement Under Consent Decree
Sunset Natural Products Inc. is recalling Thor dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.
What this means for you
Illness, injury, or structural failure has been reported. 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 significant health risk or temporary adverse health consequences.
Plain-English summary
Sunset Natural Products Inc. is recalling Thor, 60 capsules per bottle, pursuant to a consent decree entered on September 25, 2015. The decree prohibits the company and its owners from marketing dietary supplements until they recall and destroy all products manufactured, prepared, processed, packed, labeled, held, and/or distributed between April 2, 2014, and the date of the decree's entry. The firm must also hire a cGMP expert and receive written permission from the FDA to resume operations.
The recall covers 1,963 bottles (180,000 capsules) of Thor. Known lots include Lot # 051214 (Exp. Date 12/17), Lot # 160515 (Exp. Date 05/18), and Lot # 260515 (Exp. Date 05/18). The products were distributed to Florida, Nevada, and the Dominican Republic.
Consumers who have purchased these products should stop using them and follow the instructions provided by the recalling firm or the FDA regarding the destruction of the supplements under FDA supervision.
The recalled product
- Product
- Thor, 60 capsules per bottle
- 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 (13)
- 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 lots and expiration dates: Lot # 051214 Exp. Date 12/17
- Lot # 160515 Exp. Date 05/18
- Lot # 260515 Exp Date 05/18
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 · cGMP violation
See all →- HighHand Sanitizer Recalled Due to Manufacturing Practice Deviations
FDA (Drugs) · 2023-02-08
- ModeratePyrogenium Homeopathic Remedy Recalled for Manufacturing Process Violations
FDA (Drugs) · 2022-06-22
- ModerateDrug Recall: PAINAID Tablets for Manufacturing Deviations
FDA (Drugs) · 2022-02-09
- ModerateDrug Recall: PEPTIME Energy Caffeine Tablets cGMP Violations
FDA (Drugs) · 2022-02-09
- ModerateCalvin Scott Recalls Diethylpropion Tablets Due to Stability Deviations
FDA (Drugs) · 2020-10-14