Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated…
Recalling firm: Martin Bauer, Inc.
Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 9, 2026.
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FDA code information
Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25
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Full FDA record and distribution details
Original product description
Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner .
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| batch | 24008914 | Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25 |
Original FDA recall reason
Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )
Recall details
- Recall number
- H-0532-2025
- Event ID
- 97355
- FDA status
- Terminated
- Initiated
- Jul 22, 2025
- Reported
- Sep 3, 2025
- Classified
- Aug 26, 2025
- Terminated
- Feb 9, 2026
- Quantity
- 775 kg
- Location
- Secaucus, NJ, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
The recalling firm distributed the adulterated to one consignee in North Carolina.
Data updated September 16, 2026. View official FDA data ↗
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