← FDA ENFORCEMENT
H-0532-2025Class II

Martin Bauer, Inc.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Martin Bauer, Inc.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-09-03
Distribution
The recalling firm distributed the adulterated to one consignee in North Carolina.
Firm state
NJ
Product quantity
775 kg
Initiated by
Voluntary: Firm initiated
Reason for recall

Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )

Product description

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

Code / lot info

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

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →