Refreshe Lime Electrolyte Water (Sweetwater Co.) – Total Coliforms (2013)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Refreshe Lime Naturally Flavored Electrolyte Water, 12 bottles per cases, 1 L per bottle, sold under Safeway brand. The UPC 0 21130 24208 5.
Brand
The Sweetwater Co., Inc.
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Best by date 10/11/2014. S3805 0700 through 1500. S3805 - is the firm's customer information. Number 0700 through 1500 is the time the bottle was produced from 07:00 hours to 15:00 hours.
The Sweetwater Co., Inc. is recalling Refreshe Lime Naturally Flavored Electrolyte Water, 12 bottles per cases, 1 L per bottle, sold under due to Sweetwater Company recalls Refreshe Lime Naturally Flavored Electrolyte Water (1 L size) due to elevated amount of non-fecal total Coliforms.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sweetwater Company recalls Refreshe Lime Naturally Flavored Electrolyte Water (1 L size) due to elevated amount of non-fecal total Coliforms.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, IN, OR
Page updated: Jan 6, 2026