Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic l... — FDA record H-0532-2025

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 22, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

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 )
Classification
Class II
Recalling firm
Martin Bauer, Inc.
Quantity
775 kg
Agency-reported status
Terminated
Source record identifier
H-0532-2025

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityManufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

The recalling firm distributed the adulterated to one consignee in North Carolina.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Sep 3, 2025
Recall initiation date
Jul 22, 2025
Center classification date
Aug 26, 2025
Termination date
Feb 9, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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