Class IITerminated · reported 2024-10-23

Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN barcode 00850010449043.

Hydration Labs Inc. dba Bevi recalled this product and the FDA reported the enforcement action on 23 October 2024 as Class II. The recall was initiated by the firm. Product is labeled as electrolytes but is actually caffeine

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

Product: 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.
Reason for recall: Product is labeled as electrolytes but is actually caffeine
Recalling firm: Hydration Labs Inc. dba Bevi
Firm location: Charlestown, Massachusetts, United States
Classification: Class II
Status: Terminated
Recall number: F-0034-2025
Quantity: 1611 units
Distribution: Nationwide and Canada
Initiated: 6 September 2024
Reported by FDA: 23 October 2024
Terminated: 23 June 2025
Firm notified by: Letter
Product codes: TP24208A

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
This record is the only one the FDA opened for its recall event, so it covers a single product code.
The recall ran for 10 months, from 6 September 2024 to termination on 23 June 2025. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
The FDA published the enforcement report 7 weeks after the firm began the recall.
The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.

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Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.