Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN barcode 00850010449043. Product is packaged as a Bag In B
Summary
The FDA issued a Class II for Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN barcode 00850010449 by Hydration Labs Inc. dba Bevi. Reason: Product is labeled as electrolytes but is actually caffeine.
Details
Source
Food Recall
External ID
F-0034-2025
Action Date
2024-10-23
Status
Terminated
Category
food
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.
Lot/Code Info: TP24208A
Quantity Affected: 1611 units
Reason for Recall
Product is labeled as electrolytes but is actually caffeine
Distribution
Nationwide and Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2024-09-06
Company
Charlestown, MA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Hydration Labs Inc. dba Bevi) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Hydration Labs Inc. dba Bevi have FDA actions?
This is the only FDA action we have on record for Hydration Labs Inc. dba Bevi in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0034-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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