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Class IIITerminated in FDA datasetRecall initiated Jun 10, 2015

Mixed Berry Flavored Electrolyte bottled Water, sold under brand HyVee, Raleys' Purely Made,…

Recalling firm: The Sweetwater Co., Inc.

Why it was recalled

Mixed Berry Flavored Electrolyte Water is recalled due to high total coliform testing results.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Dec 30, 2015.

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Compare the exact product and package details with the label you have.

ProductMixed Berry Flavored Electrolyte bottled Water, sold under brand HyVee, Raleys' Purely Made, and Refreshe. Each bottle is 1 Liter (33.8 Fl. oz.). HyVee brand has the UPC 0 75450 12723 2; Raley's brand has the UPC 0 46567 02874 3; Refreshe has the UCP 0 21130 24209 2;
Package size1 Liter
UPC046567028743, 075450127232

FDA code information

best by dates: 051316; 051916; or 052916

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Mixed Berry Flavored Electrolyte bottled Water, sold under brand HyVee, Raleys' Purely Made, and Refreshe. Each bottle is 1 Liter (33.8 Fl. oz.). HyVee brand has the UPC 0 75450 12723 2; Raley's brand has the UPC 0 46567 02874 3; Refreshe has the UCP 0 21130 24209 2;

Extracted codes and context

TypeCode / valueContext
UPC046567028743. oz.). HyVee brand has the UPC 0 75450 12723 2; Raley's brand has the UPC 0 46567 02874 3; Refreshe has the UCP 0 21130 24209 2;
UPC075450127232d Refreshe. Each bottle is 1 Liter (33.8 Fl. oz.). HyVee brand has the UPC 0 75450 12723 2; Raley's brand has the UPC 0 46567 02874 3; Refreshe has the UCP 0 21130 24209 2;

Original FDA recall reason

Mixed Berry Flavored Electrolyte Water is recalled due to high total coliform testing results.

Recall details

Recall number
F-2771-2015
Event ID
71476
FDA status
Terminated
Initiated
Jun 10, 2015
Reported
Jul 1, 2015
Classified
Jun 25, 2015
Terminated
Dec 30, 2015
Quantity
3468 cases (12 bottles per case)
Location
Culver, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distributed in Arizona, California, Colorado, Indiana, Iowa, Oregon, Pennsylvania, Tennessee, Texas, and Washington

FDA source record · F-2771-2015

Data updated September 16, 2026. View official FDA data ↗

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