RecallHawk
Class I Recall

Gardner's Candies Cappuccino Meltaway Bar 1.25 oz. (35g), Item Number: 15207/online website item number is 0015207, sold

GARDNER'S CANDIES , INC

Summary

The FDA issued a Class I for Gardner's Candies Cappuccino Meltaway Bar 1.25 oz. (35g), Item Number: 15207/onl by GARDNER'S CANDIES , INC. Reason: Product contains Undeclared Allergen Tree Nuts (Cashews).

Details

Source

Food Recall

External ID

F-0376-2025

Action Date

2025-01-08

Status

Terminated

Category

food

Product Description

Gardner's Candies Cappuccino Meltaway Bar 1.25 oz. (35g), Item Number: 15207/online website item number is 0015207, sold individually and; also as part of Gardner's Meltaway Treat Box 6 oz, Item Number: 50135 or online website item number is 0050135

Lot/Code Info: Gardner's Cappuccino Meltaway Bar: dated 082725; Gardner's Meltaway Treat Box: dated either 101625 or 112525

Quantity Affected: 2,007 bars. 196 of the bars went into the Meltaway Treat boxes.

Reason for Recall

Product contains Undeclared Allergen Tree Nuts (Cashews)

Distribution

The recalled product was distributed to the following States: PA, OH, GA, MN, NM, MD, KY, SC, FL, MO, CA

Type: Voluntary: Firm initiated

Recall Initiated: 2024-12-10

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 63 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 (GARDNER'S CANDIES , INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does GARDNER'S CANDIES , INC have FDA actions?

This is the only FDA action we have on record for GARDNER'S CANDIES , INC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0376-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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