FDA recall record
Reishi Mushroom, 90 capsules
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 March 31, 2015. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Reishi Mushroom, 90 capsules
Reason
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
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.
Reishi Mushroom, 90 capsules
Code information listed by FDA
9671
Distribution and firm information
Recalling firm listed by FDA: Health One Pharmaceuticals Inc
Firm location listed by FDA: City Of Industry, CA, United States
Distribution reported by FDA: Nationwide in US: CA, TN, WA, ID, and worldwide: Hong Kong, Vietnam, China, Singapore
Product quantity listed by FDA: 2771 units
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.