Class IITerminatedVoluntary: Firm initiated
Martin Bauer, Inc.: food recall H-0532-2025
Martin Bauer, Inc. of Secaucus, NJ recalled Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic… Reason: Misbranding of the ingredient the firm sells ( Passionflower Herb Extract ). The FDA listed it as Class II in its Enforcement Report dated Sep 3, 2025; distribution: North Carolina.
Record status as published: Terminated (terminated Feb 9, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner .
- Product quantity
- 775 kg
- Reason for recall
- Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )
- Codes, lots and dates on the package
- Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25
- Distribution pattern
- The recalling firm distributed the adulterated to one consignee in North Carolina.
- Recalling firm
- Martin Bauer, Inc., Secaucus, NJ
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jul 22, 2025 |
| Classified by the FDA | Aug 26, 2025 |
| Published in the Enforcement Report | Sep 3, 2025 |
| Terminated | Feb 9, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0532-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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