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
- DHEA 25 mg, bulk capsules
- 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 lots and expiration dates: Lot # 140714 Exp. Date 08/17, Lot # 310914 Exp. Date 10/17, Lot # 560914 Exp. Date 10/17, Lot # 271214 Exp. Date 12/17, Lot # 070115 Exp. Date 01/18, Lot # 460315 Exp. Date 04/18, Lot # 080615 Exp. Date 08/18
- Quantity
- 1,444,900 capsules
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