FDA recall record
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...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of November 25, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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
Reason
Microcystins level found to be above the specification limit of NMT1 ppm as per Raw Material Specification.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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
Code information listed by FDA
Lot # 6E436-0; Product Code # 07596; Expiry Date: 09/2018
Distribution and firm information
Recalling firm listed by FDA: Seroyal International, a division of Atrium Innovations
Firm location listed by FDA: Richmond Hill, Ontario, Canada
Distribution reported by FDA: Product was distributed throughout the United States and Canada (see attached document for list of Canadian consignees).
Product quantity listed by FDA: 4,226 bottles (1691 Canada and 2535 USA)
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.