CLASS II Food recall · Reported 3 Sep 2025 · FDA Enforcement Report
Passionflower Herb Powdered Extract 4%, bulk packaging recalled
Martin Bauer is recalling Passionflower Herb Powdered Extract 4%, bulk packaging, individual large, corrugated, distributed in North Carolina. The recall was initiated on 22 Jul 2025 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0532-2025
- FDA event ID
- 97355
- Recalling firm
- Martin Bauer, Secaucus, NJ
- Brand
- Passionflower Herb
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 22 Jul 2025
- FDA classified
- 26 Aug 2025
- Reported
- 3 Sep 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Labeling Errors
- Product category
- Other
Timeline
| 22 Jul 2025 | Recall initiated by company | |
| 26 Aug 2025 | Classified by FDA | +35 days |
| 3 Sep 2025 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )
Product as listed by the FDA
Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner .
Where it was distributed
The recalling firm distributed the adulterated to one consignee in North Carolina.
Questions about this recall
Why was it recalled?
Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )
Which lots are affected?
Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25
Where was it sold?
The recalling firm distributed the adulterated to one consignee in North Carolina.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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