RecallHawk
Class I Recall

(BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099

Honeyville, Inc

Summary

The FDA issued a Class I for (BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099 by Honeyville, Inc. Reason: Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products..

Details

Source

Food Recall

External ID

H-0849-2026

Action Date

2026-06-03

Status

Ongoing

Category

food

Product Description

(BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099

Lot/Code Info: Lot number# 0325357B201

Quantity Affected: 4980 pounds (all on hold at customer location)

Reason for Recall

Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.

Distribution

Distribution is to California and Utah consignees.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-04-21

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 75 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Honeyville, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Honeyville, Inc have FDA actions?

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

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0849-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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