RecallHawk
Class I Recall

Walker's Wine Juice Pumpkin Juice 2.5, 5, 30, 60, 275 gallon bulk containers

Walker's Fruit Basket and Press House

Summary

The FDA issued a Class I for Walker's Wine Juice Pumpkin Juice 2.5, 5, 30, 60, 275 gallon bulk containers by Walker's Fruit Basket and Press House. Reason: May be contaminated with Clostridium botulinum.

Details

Source

Food Recall

External ID

F-0730-2025

Action Date

2025-04-30

Status

Terminated

Category

food

Product Description

Walker's Wine Juice Pumpkin Juice 2.5, 5, 30, 60, 275 gallon bulk containers

Lot/Code Info: All lots and codes

Quantity Affected: 1466 gallons

Reason for Recall

May be contaminated with Clostridium botulinum

Distribution

IL, IN, KS, KY, ME, MI, MN, NJ, NY, OH, PA, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2025-03-28

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 35 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 (Walker's Fruit Basket and Press House) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Walker's Fruit Basket and Press House have FDA actions?

This is the only FDA action we have on record for Walker's Fruit Basket and Press House in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0730-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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