FDA recalls · F-1059-2017
Sunset Natural Products Inc. recall
- FoodLibene Dietary Supplement (unknown container size)
- ReasonPursuant 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.
- ClassClass II: the food could cause temporary or treatable health problems
- StatusClosed by FDA, ended 2017-04-10
- DatesFirm started it 2015-10-13. In FDA's enforcement report 2017-01-04.
- Sold inProducts distributed to Florida, Nevada and the Dominican Republic
- AmountUnknown
- CodesAs 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: Lot # 160615
- FirmSunset Natural Products Inc., Miami, FL · FDA Mandated
Products we list
None. We tie a recall to a product only by a barcode printed in the recall, and this one names none we list. That does not mean the recalled food is missing from our listings.
From FDA's enforcement report, via openFDA (CC0): raw data for this recall. FDA's own Enforcement Report search finds it by its number, F-1059-2017. Class meanings: FDA.