Martin Bauer recalls Passionflower Herb Powdered Extract 4% bulk packaging due to misbranding of the ingredient. Consumers should check for specific packaging details to determine if affected.
Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )
Martin Bauer is recalling its Passionflower Herb Powdered Extract 4% product due to misbranding. This means the product may not be labeled correctly, which could lead to confusion about the actual ingredients.
The product is misbranded, meaning it does not accurately reflect the actual ingredients it contains. This could lead to confusion about what the product contains, potentially causing incorrect usage or health decisions.
Anyone who purchased the Passionflower Herb Powdered Extract 4% in bulk packaging from Martin Bauer. Consumers most at risk are those who rely on the product for specific herbal remedies.
Check for the corrugated cardboard box with plastic liner and the specific manufacturing batch number 24008914 from September 25, 2024. The product is sold in bulk packaging and individual large boxes.
Look for the manufacturing batch number 24008914 and date of manufacture September 25, 2024 on the packaging.
No, the product is misbranded but not hazardous. The recall is for labeling accuracy, not safety risks.
Check for the corrugated cardboard box with plastic liner and the batch number 24008914 manufactured on September 25, 2024.
The recall does not require action; consumers should check the product details to confirm if it matches the recalled batch.
We’ve drafted a message you can send Martin Bauer to request your refund or repair — edit it as you like.
Subject: Recall H-0532-2025 — Martin Bauer Martin Bauer Hello, I own a Martin Bauer that is covered by recall H-0532-2025 from Martin Bauer. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
