FDA Food recall F-1756-2018
Genestra brand AFA-gen capsule 15 mg Niacin/ capsule 300 mg Blue Green Algae / capsule 2 capsules, twice daily Dietary supplement 90 capsul…
- FDA Food
- Class II
- terminated
- Published 2018-08-15
On 2018-08-15 the FDA classified a Class II recall of Genestra brand AFA-gen capsule 15 mg Niacin/ capsule 300 mg Blue Green Algae / capsule 2 capsules, twice daily Dietary supplement 90 capsul… by Seroyal International A Division, citing microcystins level found to be above the specification limit of NMT1 ppm as per Raw Material Specification.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-1756-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-07-27 |
| Published | 2018-08-15 |
| Last updated | 2026-09-13 11:50 UTC |
| Company | Seroyal International A Division |
| Distribution | US |
Product
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.
Identifiers
| code_info | Lot # 6E436-0; Product Code # 07596; Expiry Date: 09/2018 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:50 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1756-2018%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.