RecallHawk
Class II Recall

Zen Cleanse Blend herbal tea; .95 oz (27g) pouch; 18 pouches/box UPC: 819005011504

Bell Industries LLC

Summary

The FDA issued a Class II for Zen Cleanse Blend herbal tea; .95 oz (27g) pouch; 18 pouches/box UPC: 8190050115 by Bell Industries LLC. Reason: Potential Salmonella contamination.

Details

Source

Food Recall

External ID

H-0327-2026

Action Date

2025-12-31

Status

Ongoing

Category

food

Product Description

Zen Cleanse Blend herbal tea; .95 oz (27g) pouch; 18 pouches/box UPC: 819005011504

Lot/Code Info: Lot: A8205 Expiration date: 11/2028

Quantity Affected: 66 units

Reason for Recall

Potential Salmonella contamination

Distribution

Product was distributed to 3 customers located in MA, TX WI. Product was not made available to the public and did not make it to retail shelves.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-11-24

Company

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 33 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 (Bell Industries LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Bell Industries LLC have FDA actions?

This is the only FDA action we have on record for Bell Industries LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0327-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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