Herbal Extract Recall: Martin Bauer Powdered Passionflower 4%
Announced 2025-09-03 · FDA
FDA is recalling Martin Bauer Passionflower herb powdered extract 4% in bulk packaging due to misbranding of the ingredient (Passionflower Herb Extract). The product was distributed to one consignee in North Carolina, totaling 775 kg; recall batch 24008914 manufactured 25.09.2024, recall item 0171319MBU. No corrective action is provided.
| Brand | Martin Bauer, Inc. |
|---|---|
| Product | 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 ) |
| Severity | moderate |
| Units affected | 775 |
| Distribution | The recalling firm distributed the adulterated to one consignee in North Carolina. |
| Agency | FDA |
| Recall / campaign no. | Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25 |
WHAT YOU SHOULD DO
- If you have this product, stop using it.
- Contact the distributor or Martin Bauer for instructions on return or disposal.
- Keep the product packaging for reference and monitor for any adverse effects; seek medical advice if needed.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.