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Lower risk Food recall · FDA · Published December 2, 2025

Lost and Found Energy Sour Gummy Bear Recall: Incorrect Caffeine Label

Fazt & Loud LLC recalls 12-pack Sour Gummy Bear Energy drinks due to misprinted caffeine label showing 300mg instead of 150mg. Consumers should check UPCs and lot numbers.

🇺🇸 FDA recall #H-0441-2026FoodFazt & Loud ›
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Recalling firmFazt & Loud LLC3010 Lbj Fwy Fl 1200 · Dallas, TX 75234-2710
✎ GovInfoNow plain-language explainer

Fazt & Loud LLC is recalling 12-packs of Sour Gummy Bear Energy drinks because the label incorrectly states 300mg of caffeine instead of 150mg. This misprint could lead to unintended caffeine intake, especially for sensitive individuals. Read more at govinfonow.com/recall/6927-lost-and-found-energy-sour-gummy-bear-recall-incorrect-caffeine.

Source Summary by GovInfoNow · govinfonow.com/recall/6927-lost-and-found-energy-sour-gummy-bear-recall-incorrect-caffeine · Updated August 17, 2026 · Official notice: FDA #H-0441-2026

Cite this page

“Lost and Found Energy Sour Gummy Bear Recall: Incorrect Caffeine Label.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6927-lost-and-found-energy-sour-gummy-bear-recall-incorrect-caffeine. Based on FDA recall #H-0441-2026.

The FDA announced on Dec. 2, 2025, that Fazt & Loud LLC voluntarily recalled Lost and Found Energy Sour Gummy Bear cans due to a label misprint showing incorrect caffeine content. Consumers should stop consuming the product immediately.

How to tell if you have it

  • Brand: Fazt & Loud
  • Product: Lost and Found Energy, Sour Gummy Bear, 12pck, 16oz Cans Case UPC: 850075595655 Can UPC: 850075595662 Aluminum Can
  • Lot #: MO-00911
  • BB Date: 11/13/2027
  • UPC: 00850075595655
  • UPC: 00850075595662

The hazard

The 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.

Context

GovInfoNow's records show other recent recalls include Gimme Coffee Decaf Pods Recall: Undeclared Caffeine Hazard (2025-11-24) and Shaman Botanicals Recalls White Vein Chewable Tablets Due to Dosage Error (2026-02-13). Prospector Popcorn Recall: Nutrient Labeling Error was reported on 2026-07-15.

How to tell if you have this one

Check for the UPC 850075595655 or 850075595662 on the product case. The lot number is MO-00911 BB with a date of 11/13/2027.

  • Brand
    Fazt & Loud
  • Product
    Lost and Found Energy, Sour Gummy Bear, 12pck, 16oz Cans Case UPC: 850075595655 Can UPC: 850075595662 Aluminum Can
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the UPC code on the product case (850075595655 or 850075595662) and lot number (MO-00911 BB).

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 2 months after the firm started it.

1. Firm started the recall: Dec 2, 202512. FDA classified it Class III: Feb 2, 202623. Published in FDA’s Enforcement Report: Feb 11, 2026320252026
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

What should I do if I have the recalled product?

The recall does not require immediate action, but you should check the product details to confirm if it's affected.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-0441-2026 (December 2, 2025)
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA