Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Genestra brand AFA-gen capsule 15 mg Niacin/ capsule 300 mg Recalled by Seroyal International, a division of Atrium Innovations Due to Microcystins level found to be above the specification...

Date: July 27, 2018
Company: Seroyal International, a division of Atrium Innovations
Status: Terminated
Source: FDA (Food)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Seroyal International, a division of Atrium Innovations directly.

Affected Products

Genestra brand AFA-gen capsule 15 mg Niacin/ capsule 300 mg Blue Green Algae / capsule 2 capsules, twice daily Dietary supplement 90 capsules, White 150cc HDPE Bottle with Desiccant and white cap, packed as 12 bottles / shipper case

Quantity: 4,226 bottles (1691 Canada and 2535 USA)

Why Was This Recalled?

Microcystins level found to be above the specification limit of NMT1 ppm as per Raw Material Specification.

Where Was This Sold?

Product was distributed throughout the United States and Canada (see attached document for list of Canadian consignees).

About Seroyal International, a division of Atrium Innovations

Seroyal International, a division of Atrium Innovations has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Food). Last updated March 26, 2026. View original report