RecallRadar

FDA Food recall F-0995-2017

Aloe Vera & Lecithin, bulk capsules

On 2017-01-04 the FDA classified a Class II recall of Aloe Vera & Lecithin, bulk capsules by Sunset Natural Products, citing 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….

Read the official FDA Food notice

AgencyFDA Food
Recall numberF-0995-2017
ClassificationClass II
Statusterminated
Initiated2015-10-13
Published2017-01-04
Last updated2026-09-13 11:49 UTC
CompanySunset Natural Products
DistributionFL, NV

Product

Aloe Vera & Lecithin, bulk capsules

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.

Identifiers

code_info
As persuant to the Consent Decree, the firm agreed to "recall and destroy, under FDA's supervision, in accordance with…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 # 630714 Exp. Date 07/17, Lot # 42914 Exp. Date 10/17, Lot # 430914 Exp. Date 10/17, Lot # 10114 Exp. Date 12/17, Lot # 210215 Exp. Date 03/18, Lot # 370515 Exp. Date 06/18, Lot # 050815 Exp. Date 08/18, Lot # 281114 Exp. Date 12/17

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:49 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0995-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.