Home / Recalls / Sunset Natural Products Inc. / F-0933-2017

F-0933-2017 Class II Terminated

Recalled by Sunset Natural Products Inc. — Miami, FL

FDA food recall F-0933-2017 was initiated by Sunset Natural Products Inc. on Oct 13, 2015 and is designated Class II. 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… The recall status is terminated (terminated Apr 10, 2017). Affected quantity: 3,000,000 capsules.

Recall Details

Product Type
Food
Report Date
Jan 4, 2017
Initiation Date
Oct 13, 2015
Termination Date
Apr 10, 2017
Voluntary/Mandated
FDA Mandated
Product Quantity
3,000,000 capsules

Product Description

Artrosamin, 250,000 capsules per bulk order

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.

Distribution Pattern

Products distributed to Florida, Nevada and the Dominican Republic

Code Information

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 # 030414 Exp. Date 04/17, Lot # 040414 Exp. Date 04/17, Lot # 050414 Exp. Date 04/17, Lot # 060414 Exp. Date 04/17, Lot # 070414 Exp. Date 04/17, Lot # 080414 Exp. Date 04/17, Lot # 010514 Exp. Date 04/17, Lot # 080514 Exp. Date 04/17, Lot # 090514 Exp. Date 04/17, Lot # 100514 Exp. Date 05/17, Lot # 110514 Exp. Date 05/17, Lot # 120514 Exp. Date 05/17,

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0933-2017
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 23, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Other recalls by Sunset Natural Products Inc.

  • F-0984-2017 Class II — Seral, bulk capsules (Oct 13, 2015)
  • F-0993-2017 Class II — Abte, bulk capsules (Oct 13, 2015)
  • F-0926-2017 Class II — Madre Cell, 60 capsules per bottle (Oct 13, 2015)
  • F-1015-2017 Class II — Sugar Burner Dietary Supplement (unknown container size) (Oct 13, 2015)
  • F-1080-2017 Class II — Glow Dietary Supplement (unknown container size) (Oct 13, 2015)
  • F-1026-2017 Class II — Prostamax Dietary Supplement (unknown container size) (Oct 13, 2015)
  • F-0958-2017 Class II — Chardon De Marie, 60 capsules per bottle (Oct 13, 2015)
  • F-0995-2017 Class II — Aloe Vera & Lecithin, bulk capsules (Oct 13, 2015)
  • F-1056-2017 Class II — Denta capsule Dietary Supplement (unknown container size) (Oct 13, 2015)
  • F-0920-2017 Class II — Crea Care, (100,000 capsule bulk) (Oct 13, 2015)

FDA data resources