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Food FDA Class I Terminated Undeclared allergen

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

GARDNER'S CANDIES , INC Published Jan 8, 2025

Risk level

Class I

Dangerous or defective — could cause serious health problems or death.

Severity score 87/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • If you are allergic or sensitive to the ingredient noted, do not eat it — it could cause a serious reaction.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact GARDNER'S CANDIES , INC or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Product contains Undeclared Allergen Tree Nuts (Cashews)

Hazards

Tree Nuts · primary

Affected products (1)

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

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

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

Affected areas

CaliforniaFloridaGeorgiaKentuckyMarylandMinnesotaMissouriNew MexicoOhioPennsylvaniaSouth Carolina

Timeline

  1. Initiated
    Dec 10, 2024
  2. Published
    Jan 8, 2025
  3. Terminated
    Feb 20, 2025
Recall number
F-0376-2025
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.