Passionflower Herb Powdered Extract 4% recall
Recalled by Martin Bauer, Inc. · Secaucus, NJ, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner .
Quantity: 775 kg
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25
Where it was sold
North Carolina
FDA's distribution note: The recalling firm distributed the adulterated to one consignee in North Carolina.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Martin Bauer, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 22, 2025
- In FDA report of
- Sep 3, 2025
- Terminated
- Feb 9, 2026
- FDA recall number
- H-0532-2025 · event 97355
- Official record
- FDA enforcement report search