Why it was recalled
Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )
Product description
Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner .
Lot numbers, UPCs & expiration codes
Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25
Where it was sold
The recalling firm distributed the adulterated to one consignee in North Carolina.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- H-0532-2025
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Jul 22, 2025
- FDA report date
- Sep 3, 2025
- Quantity
- 775 kg
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Martin Bauer, Inc.
Original FDA data
Every field from FDA enforcement report H-0532-2025, exactly as published.
Show all FDA fields
- City
- Secaucus
- State
- NJ
- Status
- Terminated
- Country
- United States
- Event ID
- 97355
- Address
- 400 Plaza Dr Fl 3
- Code information
- Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25
- Postal code
- 07094-3605
- Report date
- Sep 3, 2025
- Product type
- Food
- Recall number
- H-0532-2025
- Classification
- Class II
- Recalling firm
- Martin Bauer, Inc.
- Product quantity
- 775 kg
- Termination date
- Feb 9, 2026
- Reason for recall
- Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner .
- Distribution pattern
- The recalling firm distributed the adulterated to one consignee in North Carolina.
- Recall initiation date
- Jul 22, 2025
- Initial firm notification
- Center classification date
- Aug 26, 2025