CLASS I Food recall · Reported 8 Jan 2025 · FDA Enforcement Report
Cappuccino Meltaway Bar recalled by Gardner's Candies
Gardner's Candies is recalling Cappuccino Meltaway Bar, distributed in 11 states. The recall was initiated on 10 Dec 2024 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0376-2025
- FDA event ID
- 95972
- Recalling firm
- Gardner's Candies, Tyrone, PA
- Brand
- Gardner's Candies
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 10 Dec 2024
- FDA classified
- 2 Jan 2025
- Reported
- 8 Jan 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Tree Nuts
- Product category
- Candy
Timeline
| 10 Dec 2024 | Recall initiated by company | |
| 2 Jan 2025 | Classified by FDA | +23 days |
| 8 Jan 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product contains Undeclared Allergen Tree Nuts (Cashews)
Product as listed by the FDA
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
Where it was distributed
The recalled product was distributed to the following States: PA, OH, GA, MN, NM, MD, KY, SC, FL, MO, CA
CaliforniaFloridaGeorgiaKentuckyMarylandMinnesotaMissouriNew MexicoOhioPennsylvaniaSouth Carolina
Questions about this recall
Why was it recalled?
Product contains Undeclared Allergen Tree Nuts (Cashews)
Which lots are affected?
Gardner's Cappuccino Meltaway Bar: dated 082725; Gardner's Meltaway Treat Box: dated either 101625 or 112525
Where was it sold?
The recalled product was distributed to the following States: PA, OH, GA, MN, NM, MD, KY, SC, FL, MO, CA
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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