Honey Caramels Creamy Fudge. Net wt. 5.87. PLU Code: 788394 12354 2.
Summary
The FDA issued a Class II for Honey Caramels Creamy Fudge. Net wt. 5.87. PLU Code: 788394 12354 2. by Queen Bee Gardens, LLC. Reason: Products may potentially contain one or more of the following undeclared tree nuts: Pecans, Almonds, Coconut, Macadamia Nuts, & Walnuts..
Details
Source
Food Recall
External ID
F-1476-2022
Action Date
2022-07-27
Status
Terminated
Category
food
Product Description
Honey Caramels Creamy Fudge. Net wt. 5.87. PLU Code: 788394 12354 2.
Lot/Code Info: None
Quantity Affected: 717 pieces
Reason for Recall
Products may potentially contain one or more of the following undeclared tree nuts: Pecans, Almonds, Coconut, Macadamia Nuts, & Walnuts.
Distribution
Ten retail locations owned by Queen Bee in CO, NM, WY and nationwide via internet sales.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-04-28
Company
Lovell, WY
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 88 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Queen Bee Gardens, LLC has 49 FDA actions in our database, including 49 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 (Queen Bee Gardens, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Queen Bee Gardens, LLC have FDA actions?
Queen Bee Gardens, LLC has 49 FDA actions in our database, including 49 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1476-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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