martin bauer, inc.foodHigh PriorityExpired

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

martin bauer, inc. Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner . was recalled by the FDA. Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )

By RecallRadar Editorial Team

Sourced from FDA. Last reviewed March 4, 2026.

This recall involves safety concerns. Take action promptly.

✨ Plain-English Summary

Is This Recall Still Active?

Status: No - Expired

This recall is no longer active. You can still review details here for historical reference and confirmation.

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source: FDA
Announced by source: July 22, 2025
Last reviewed by RecallRadar: March 4, 2026

What You Should Do

1## Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner . Agency: FDA | Category: food | Date: 2025-07-22 Reason: Misbranding of the ingredient the firm sells ( Passionflower Herb Extract ) What to do:
2Stop using the product if it matches your lot/model.
3Compare your product details with the FDA recall notice.
4Follow the manufacturer's remedy instructions (refund, replacement, or disposal).

Open Official Recall Notice Make sure you're covered for future martin bauer, inc. recalls

What's Being Recalled

Quoted source excerpt from the official notice.

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

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

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

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

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

Frequently Asked Questions

Is my martin bauer, inc. device affected?

Check the affected models section on this page. The official notice currently lists Manufacturing Finzelberg Item: 0171319MBU Manufacturing Finzelberg Batch: 24008914 Manufactured: 25.09.2024 Quantity KG: 25.

What is the remedy for this recall?

## Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner . Agency: FDA | Category: food | Date: 2025-07-22 Reason: Misbranding of the ingredient the firm sells ( Passionflower Herb Extract ) What to do: 1. Stop using the product if it matches your lot/model. 2. Compare your product details with the FDA recall notice. 3. Follow the manufacturer's remedy instructions (refund, replacement, or disposal).

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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