CLASS II Food recall · Reported 30 Nov 2022 · FDA Enforcement Report
Gfuel Watermelon Limeade Energy Drink recalled
G Fuel is recalling Gfuel Watermelon Limeade Energy Drink;; ready-to-drink energy beverage in a, distributed nationwide in the US. The recall was initiated on 18 Oct 2022 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0166-2023
- FDA event ID
- 91107
- Recalling firm
- G Fuel, West Babylon, NY
- Brand
- Gfuel Watermelon
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 18 Oct 2022
- FDA classified
- 21 Nov 2022
- Reported
- 30 Nov 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Energy Drinks
Timeline
| 18 Oct 2022 | Recall initiated by company | |
| 21 Nov 2022 | Classified by FDA | +34 days |
| 30 Nov 2022 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product label does not declare the correct amount of caffeine.
Product as listed by the FDA
GFUEL brand Watermelon Limeade Energy Drink; 16 fl. oz.; ready-to-drink energy beverage in a can
Where it was distributed
Nationwide.
Questions about this recall
Why was it recalled?
Product label does not declare the correct amount of caffeine.
Which lots are affected?
Lot no: 0002911440 Best By: 08/16/2024
Where was it sold?
Nationwide.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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