The GFB Gluten Free Bites Dark Chocolate and Coconut 1.2oz. UPC 856818008895, 10 retail units per tray, 6 trays per whol
Summary
The FDA issued a Class I for The GFB Gluten Free Bites Dark Chocolate and Coconut 1.2oz. UPC 856818008895, 10 by West Thomas Partners, LLC. dba Gluten Free Bar. Reason: Undeclared cashews.
Details
Source
Food Recall
External ID
F-1733-2022
Action Date
2022-09-21
Status
Terminated
Category
food
Product Description
The GFB Gluten Free Bites Dark Chocolate and Coconut 1.2oz. UPC 856818008895, 10 retail units per tray, 6 trays per wholesale case.
Lot/Code Info: Case lot 041323 1.2oz unit lot 041323-174
Quantity Affected: 349 cases
Reason for Recall
Undeclared cashews
Distribution
AL AR CA CO FL IL MA ME MI MN Ms MT NC NV NY OK OR PA PA TN TX UT VA WA WI WY
Type: Voluntary: Firm initiated
Recall Initiated: 2022-08-16
Company
Grand Rapids, MI
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 49 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (West Thomas Partners, LLC. dba Gluten Free Bar) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does West Thomas Partners, LLC. dba Gluten Free Bar have FDA actions?
This is the only FDA action we have on record for West Thomas Partners, LLC. dba Gluten Free Bar in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1733-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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