Summary
The FDA issued a Class II for Tony's Chocolonely Dark Chocolate Almond Sea Salt by TONY'S CHOCOLONELY INC. Reason: Contains foreign objects (stones).
Details
Source
Food Recall
External ID
F-0714-2025
Action Date
2025-04-23
Status
Terminated
Category
food
Product Description
Tony's Chocolonely Dark Chocolate Almond Sea Salt
Lot/Code Info: Lot/Unit Numbers: 163094 and 162634 Expiration date(s) or Use by Date(s) or expected shelf life of product: 163094 (2-Apr-26) and 162634 (28-Feb-26) UPC Codes: 858010005641 Other Coding: 858010005658 (distribution unit)
Quantity Affected: 12,668.5 cases (190,027 individual retail units)
Reason for Recall
Contains foreign objects (stones)
Distribution
nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-01
Company
New York, NY
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 25 food recalls issued in the same week, part of 204 food-related FDA actions this month.
TONY'S CHOCOLONELY INC has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (TONY'S CHOCOLONELY INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does TONY'S CHOCOLONELY INC have FDA actions?
TONY'S CHOCOLONELY INC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0714-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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