WHY THIS PRODUCT IS LISTED
Other / see reason
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 description & recall reason
The source gives a detailed recall reason; read the complete reason and official notice before drawing conclusions about the product’s claims.
Based on the official recall record; packaging and sales claims have not been verified. Verify with the official source ↗
Identify the product
- Product description
- Pinateina
- Brand
- Not supplied by this source
- Lot, batch, UPC & other codes
- 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, 2014 and the date of entry of this Decree." The Decree was entered on September 25, 2015. Known lot and expiration date: Lot # 550315 Exp. Date 04/18
- Quantity
- 500 Bottles
Where it came from & where it went
- Recalling firm
- Sunset Natural Products Inc.
- Recalling firm address
- 7345 SW 45th St; N/A; Miami; FL; 33155-4509; United States
- Product production / origin location
- Not supplied by this source
- Distribution — source wording
- Products distributed to Florida, Nevada and the Dominican Republic
States identified in the source
Florida, Nevada
State matching is derived from the source’s distribution wording, which may be incomplete. The recalling company’s address is not used as the distribution location.
A recalling firm’s address is not necessarily where the food was grown or manufactured. Distribution can change; check the official notice.
The dates, separated
- Recall initiated
- Oct 13, 2015
- Notice published
- Not supplied
- Enforcement report
- Jan 4, 2017
- Agency classification
- Dec 28, 2016
- Source termination date
- Apr 10, 2017
- Last retrieved here
- Sep 28, 2026
FDA’s enforcement status is historical and may not reflect the current recall lifecycle. A terminated recall does not certify a product as safe.
Record provenance & interpretation
- Source identifier
- F-0966-2017
- Agency event identifier
- 74054
- Status as supplied (not live status)
- Terminated
- Category assignment
- Inferred from product text; not an agency classification.
- State matching
- Official distribution wording; locations are extracted only from distribution evidence, not company addresses. Coverage may be incomplete.
- Source dataset date
- Sep 25, 2026