GARDNER'S CANDIES , INC Recall: Product contains Undeclared Allergen Tree Nuts (Cashews)
United States
TerminatedClass I
- Company
- GARDNER'S CANDIES , INC
- Product
- Gardner's Candies Cappuccino Meltaway Bar 1.25 oz. (35g), It…
- Recall date
- December 10, 2024
- Terminated
- February 20, 2025
- Source
- FDA
Reason for recall
Product contains Undeclared Allergen Tree Nuts (Cashews)
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 2,007 bars. 196 of the bars went into the Meltaway Treat boxes. | Gardner's Cappuccino Meltaway Bar: dated 082725; Gardner's Meltaway Treat Box: dated either 101625 or 112525 |
Distribution
- The recalled product was distributed to the following States: PA
- OH
- GA
- MN
- NM
- MD
- KY
- SC
- FL
- MO
- CA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0376-2025
- Event ID
- 95972
- Status
- Terminated
- Classification
- Class I
- Company
- GARDNER'S CANDIES , INC
- 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
- Quantity
- 2,007 bars. 196 of the bars went into the Meltaway Treat boxes.
- Reason
- Product contains Undeclared Allergen Tree Nuts (Cashews)
- Recall initiation date
- December 10, 2024
- Report date
- January 8, 2025
- Classification date
- Not published in this source record
- Termination date
- February 20, 2025
- Distribution pattern
- The recalled product was distributed to the following States: PA, OH, GA, MN, NM, MD, KY, SC, FL, MO, CA
- UPC, lot, and code information
- Gardner's Cappuccino Meltaway Bar: dated 082725; Gardner's Meltaway Treat Box: dated either 101625 or 112525
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: GARDNER'S CANDIES , INC
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Pennsylvania | 1 |
| Ohio | 1 |
| Georgia | 1 |
| Minnesota | 1 |
| New Mexico | 1 |
| Maryland | 1 |
| Kentucky | 1 |
| South Carolina | 1 |
| Florida | 1 |
| Missouri | 1 |
| California | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
