FDA recall record
Heart-Plus, No. 83, 120 Capsules, Dietary Supplement
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 October 17, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Heart-Plus, No. 83, 120 Capsules, Dietary Supplement
Reason
Undeclared allergens: soy (lecithin)
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.
Heart-Plus, No. 83, 120 Capsules, Dietary Supplement
Code information listed by FDA
Lot 40800915 & 44300217
Distribution and firm information
Recalling firm listed by FDA: NatureAll-STF Holding, LLC
Firm location listed by FDA: Salt Lake City, UT, United States
Distribution reported by FDA: Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.
Product quantity listed by FDA: 598 bottles.
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.