Venocell (Sunset Natural Products) – Marketing Violation (2015)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Venocell, sold in bulk of 50,000 capsules.
Brand
Sunset Natural Products Inc.
Lot Codes / Batch Numbers
Lot # 160614 Exp. Date 06/17 and Lot # 490914 Exp. Date 10/17
Products Sold
Lot # 160614 Exp. Date 06/17 and Lot # 490914 Exp. Date 10/17
Sunset Natural Products Inc. is recalling Venocell, sold in bulk of 50,000 capsules. due to Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and de. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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 manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
FL, NV
Page updated: Jan 6, 2026