Keats London Vegan Hazelnut Dark Chocolate in a 4.93-ounce round green plastic package.
Summary
The FDA issued a Class I for Keats London Vegan Hazelnut Dark Chocolate in a 4.93-ounce round green plastic by The TJX Companies, Inc.. Reason: Product(s) may contain undeclared milk..
Details
Source
Food Recall
External ID
F-1260-2022
Action Date
2022-06-15
Status
Terminated
Category
food
Product Description
Keats London Vegan Hazelnut Dark Chocolate in a 4.93-ounce round green plastic package.
Lot/Code Info: All product codes.
Quantity Affected: 18,880 units (total)
Reason for Recall
Product(s) may contain undeclared milk.
Distribution
AL, CT, ID, LA, MN, ND, NV, PA, TN, WA, AR, DE, IL, MA, MO, NE, NY, PR, TX, WI, AZ, FL, IN, MD, MS, NH, OH, RI, UT, WV, CA, GA, KS, ME, MT, NJ, OK, SC, VA, WY, CO, IA, KY, MI, NC, NM, OR, SD, VT
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-01
Company
Framingham, MA
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 197 food recalls issued in the same week, part of 204 food-related FDA actions this month.
The TJX Companies, Inc. has 3 FDA actions in our database, including 3 recalls.
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 (The TJX Companies, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The TJX Companies, Inc. have FDA actions?
The TJX Companies, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1260-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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