Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended use: spread. Item is shelf stable. Packaging type: Jar. Net
Summary
The FDA issued a Class II for Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended use: spread. Item is by QUEEN BEE GARDENS. Reason: Product may have small flakes of stainless steel in product..
Details
Source
Food Recall
External ID
H-0383-2025
Action Date
2025-08-13
Status
Terminated
Category
food
Product Description
Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended use: spread. Item is shelf stable. Packaging type: Jar. Net wt., 11oz. UPC: 788394182006. Firm Name: Queen Bee Gardens Firm Address: 262 East Main Street, Lovell, WY 82431
Lot/Code Info: Pure Lot # 206235
Quantity Affected: Pure:112 jars
Reason for Recall
Product may have small flakes of stainless steel in product.
Distribution
Distributed Nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-16
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 108 food recalls issued in the same week, part of 204 food-related FDA actions this month.
QUEEN BEE GARDENS has 3 FDA actions in our database, including 3 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) 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 have FDA actions?
QUEEN BEE GARDENS 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 "H-0383-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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