Lost and Found Energy, Sour Gummy Bear, 12pck, 16oz Cans Case UPC: 850075595655 Can UPC: 850075595662 Aluminum Can Packa
Summary
The FDA issued a Class III for Lost and Found Energy, Sour Gummy Bear, 12pck, 16oz Cans Case UPC: 850075595655 by Fazt & Loud LLC. Reason: Recall is due to a misprint on the label that incorrectly identifies the total caffeine content on the can. The item contains 300mg of caffeine, inste.
Details
Source
Food Recall
External ID
H-0441-2026
Action Date
2026-02-11
Status
Ongoing
Category
food
Product Description
Lost and Found Energy, Sour Gummy Bear, 12pck, 16oz Cans Case UPC: 850075595655 Can UPC: 850075595662 Aluminum Can Packaged
Lot/Code Info: LOT #: MO-00911 BB Date: 11/13/2027
Quantity Affected: N/A
Reason for Recall
Recall is due to a misprint on the label that incorrectly identifies the total caffeine content on the can. The item contains 300mg of caffeine, instead of 150mg as provided on the can.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-02
Company
Dallas, TX
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Fazt & Loud LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Fazt & Loud LLC have FDA actions?
This is the only FDA action we have on record for Fazt & Loud LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0441-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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