Food Recall Check
Class II · Moderate risk Terminated Initiated Jul 27, 2018 (8 years ago)

Genestra brand AFA-gen capsule 15 mg Niacin/ capsule 300 mg Blue… recall

Recalled by Seroyal International, a division of Atrium Innovations · Richmond Hill, Ontario, Canada

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

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)

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot # 6E436-0; Product Code # 07596; Expiry Date: 09/2018

Where it was sold

Nationwide.

FDA's distribution note: Product was distributed throughout the United States and Canada (see attached document for list of Canadian consignees).

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Seroyal International, a division of Atrium Innovations
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 27, 2018
In FDA report of
Aug 15, 2018
Terminated
Nov 25, 2020
FDA recall number
F-1756-2018 · event 80661
Official record
FDA enforcement report search

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