FDA recall record
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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 July 2, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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Reason
Routine quality testing identified elevated levels of lead above applicable 2232 levels, which may pose potential health risks to a portion of the population.
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.
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Code information listed by FDA
Batch # SC698 SC698 SC686 SC692 SC683 SC680 SC658 SC665 SC658 SC658 SC629 SC613 SC607 SC587 SC583 SC576 SC566 SC560 SC556 SC543 SC532 SC527 SC519 SC507
Distribution and firm information
Recalling firm listed by FDA: NUTRANEXT BUSINESS LLC
Firm location listed by FDA: Sunrise, FL, United States
Distribution reported by FDA: US and Foreign Consignees only. No government consignees.
Product quantity listed by FDA: 6144 pkgs
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.