FDA recall record
Bulk 877 HOLISTIC DIGESTIVE MULTI packaged in poly bags within fiber drums (SKU 90461)
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 3, 2015. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Bulk 877 HOLISTIC DIGESTIVE MULTI packaged in poly bags within fiber drums (SKU 90461)
Reason
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
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.
Bulk 877 HOLISTIC DIGESTIVE MULTI packaged in poly bags within fiber drums (SKU 90461)
Code information listed by FDA
Lot #'s: 90461064, 90461065, 90461066, 90461067, and 90461068
Distribution and firm information
Recalling firm listed by FDA: National Enzyme Co
Firm location listed by FDA: Forsyth, MO, United States
Distribution reported by FDA: Domestic distribution of the product is nationwide with direct accounts in 27 states in all geographical regions. Foreign distribution consists of direct accounts in the following countries: Canada, China, Malaysia, Norway, Slovakia, South Korea, Sweden, Taiwan, and the United Kingdom.
Product quantity listed by FDA: 4,572,176 capsules
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.