CLASS II Food recall · Reported 23 Oct 2024 · FDA Enforcement Report
Flavor#115 Electrolytes, Net Contents, #740 recalled by Hydration Labs
Hydration Labs is recalling Flavor#115 Electrolytes, Net Contents, #740-0115, distributed nationwide in the US. The recall was initiated on 6 Sep 2024 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-0034-2025
- FDA event ID
- 95347
- Recalling firm
- Hydration Labs, Charlestown, MA
- Brand
- Flavor
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 6 Sep 2024
- FDA classified
- 15 Oct 2024
- Reported
- 23 Oct 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Product category
- Energy Drinks
Timeline
| 6 Sep 2024 | Recall initiated by company | |
| 15 Oct 2024 | Classified by FDA | +39 days |
| 23 Oct 2024 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product is labeled as electrolytes but is actually caffeine
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN barcode 00850010449043. Product is packaged as a Bag In Box (BIB) single unit for use in Bevi Smart Water Cooler machines dispensing flavored waters.
Where it was distributed
Nationwide and Canada
Questions about this recall
Why was it recalled?
Product is labeled as electrolytes but is actually caffeine
Which lots are affected?
TP24208A
Where was it sold?
Nationwide and Canada
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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