FDA recall record

Hydration Labs Inc. dba Bevi Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN recall — FDA F-0034-2025

Product is labeled as electrolytes but is actually caffeine

Class IIclassification
F-0034-2025official record ID
Oct 23, 2024report date

Recall record at a glance

Official recordF-0034-2025
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHydration Labs Inc. dba Bevi
Report dateOct 23, 2024
Recall initiation dateSep 6, 2024
Quantity1611 units
LocationCharlestown, MA, United States

Official 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.

Why the product was recalled

Product is labeled as electrolytes but is actually caffeine

Distribution information

Nationwide and Canada

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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