Food recall

Martin Bauer, Inc. recall: Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic...

Martin Bauer, Inc., of Secaucus, NJ, recalled Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic.... The FDA's reason: “Misbranding of the ingredient the firm sells ( Passionflower Herb Extract ).” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on July 22, 2025, and the FDA first listed it in its Enforcement Report of September 3, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

See FDA's words below

Status

Terminated

Closed February 9, 2026

The recall

Company
Martin Bauer, Inc. (Secaucus, NJ)
Reason, in FDA's words
“Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )”
Where it was sold
The recalling firm distributed the adulterated to one consignee in North Carolina.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
97355

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0532-2025 Class II

    Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner .

    Codes: Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25

    Quantity: 775 kg

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of September 3, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.