RecallHawk
Class II Recall

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

Martin Bauer, Inc.

Summary

The FDA issued a Class II for Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, co by Martin Bauer, Inc.. Reason: Misbranding of the ingredient the firm sells ( Passionflower Herb Extract ).

Details

Source

Food Recall

External ID

H-0532-2025

Action Date

2025-09-03

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25

Quantity Affected: 775 kg

Reason for Recall

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

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2025-07-22

Company

Martin Bauer, Inc.

Secaucus, NJ

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 43 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Martin Bauer, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Martin Bauer, Inc. have FDA actions?

This is the only FDA action we have on record for Martin Bauer, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0532-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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