Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported January 4, 2017
Anim Dietary Supplement (unknown container size)
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…
The recall
Sunset Natural Products Inc. issued this moderate-severity FDA Food recall — Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements unti….
- Moderate
- severity level
- Class II
- classification
- January 4, 2017
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1057-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1057-2017) was formally reported on January 4, 2017, with the manufacturer initiating the action on October 13, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Sunset Natural Products Inc. is listed as the recalling firm, operating out of Miami, FL. Federal records list the affected scope as Unknown.
The documented reason for this recall is: 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 distribu… Distribution data in the federal record shows the product reached: Products distributed to Florida, Nevada and the Dominican Republic. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category — 711 dietary supplements recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.
Affected scope
Unknown
Related Recalls
6
5 from same agency
Product description
Anim Dietary Supplement (unknown container size)
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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1057-2017 |
| Date reported | January 4, 2017 |
| Date initiated | October 13, 2015 |
| Recalling firm | Sunset Natural Products Inc. |
| Firm location | Miami, FL |
| Affected scope | Unknown |
| Distribution | Products distributed to Florida, Nevada and the Dominican Republic |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
Frequently Asked Questions
What product was recalled? ▼
Anim Dietary Supplement (unknown container size). Recalled by Sunset Natural Products Inc.. Units affected: Unknown.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on January 4, 2017. Severity: Moderate. Recall number: F-1057-2017.
Where was the recalled product distributed? ▼
Distribution: Products distributed to Florida, Nevada and the Dominican Republic.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1057-2017) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported January 4, 2017.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).