FDA recall record
Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner .
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 February 9, 2026. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner .
Reason
Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )
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.
Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner .
Code information listed by FDA
Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25
Distribution and firm information
Recalling firm listed by FDA: Martin Bauer, Inc.
Firm location listed by FDA: Secaucus, NJ, United States
Distribution reported by FDA: The recalling firm distributed the adulterated to one consignee in North Carolina.
Product quantity listed by FDA: 775 kg
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.