Hydration Labs Inc. dba Bevi Recall: Product is labeled as electrolytes but is actually caffeine
United States
TerminatedClass II
- Company
- Hydration Labs Inc. dba Bevi
- Product
- Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN…
- Recall date
- September 6, 2024
- Terminated
- June 23, 2025
- Source
- FDA
Reason for recall
Product is labeled as electrolytes but is actually caffeine
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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. | Not published in this source record | 1611 units | TP24208A |
Distribution
- Nationwide and Canada
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0034-2025
- Event ID
- 95347
- Status
- Terminated
- Classification
- Class II
- Company
- Hydration Labs Inc. dba Bevi
- Product description
- 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.
- Quantity
- 1611 units
- Reason
- Product is labeled as electrolytes but is actually caffeine
- Recall initiation date
- September 6, 2024
- Report date
- October 23, 2024
- Classification date
- Not published in this source record
- Termination date
- June 23, 2025
- Distribution pattern
- Nationwide and Canada
- UPC, lot, and code information
- TP24208A
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Hydration Labs Inc. dba Bevi
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
