Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported December 11, 2013
Refreshe Mixed Berry Naturally Flavored Electrolyte Water, 12 bottles per cases, 1 L per bottle, sold under Safeway brand. The UPC 0 21130 24209 2.
Sweetwater Company recalls Refreshe Mixed Berry Naturally Flavored Electrolyte Water (1 L size) due to elevated amount of non-fecal total Coliforms.
Compiled from official public sources by the editorial team.
Verify with FDA Food →
The Sweetwater Co., Inc. recalled Refreshe Mixed Berry Naturally Flavored Electrolyte Water, 12 bottles per cases, 1 L per … - a moderate-severity action.
Refreshe Mixed Berry Naturally Flavored Electrolyte Water, 12 bottles per cases, 1 L per … was recalled by The Sweetwater Co., Inc. in December 11, 2013. Reason: Sweetwater Company recalls Refreshe Mixed Berry Naturally Flavored Electrolyte Water (1 L size) due to elevat…. Check the official notice for the remedy. Verify recall #F-0723-2014 with the FDA Food before acting.
The recall
The Sweetwater Co., Inc. issued this moderate-severity FDA Food recall-Sweetwater Company recalls Refreshe Mixed Berry Naturally Flavored Electrolyte Water (1 L size) due to elevat….
- Moderate
- severity level
- Class II
- classification
- December 11, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0723-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0723-2014) was formally reported on December 11, 2013, with the manufacturer initiating the action on October 24, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. The Sweetwater Co., Inc. is listed as the recalling firm, operating out of Culver, OR. Federal records list the affected scope as 748 cases.
The documented reason for this recall is: Sweetwater Company recalls Refreshe Mixed Berry Naturally Flavored Electrolyte Water (1 L size) due to elevated amount of non-fecal total Coliforms. Distribution data in the federal record shows the product reached: distributed in CA and OR.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
748 cases
Related Recalls
6
0 from same agency
Product description
Refreshe Mixed Berry Naturally Flavored Electrolyte Water, 12 bottles per cases, 1 L per bottle, sold under Safeway brand. The UPC 0 21130 24209 2.
Reason for recall
Sweetwater Company recalls Refreshe Mixed Berry Naturally Flavored Electrolyte Water (1 L size) due to elevated amount of non-fecal total Coliforms.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0723-2014 |
| Date reported | December 11, 2013 |
| Date initiated | October 24, 2013 |
| Recalling firm | The Sweetwater Co., Inc. |
| Firm location | Culver, OR |
| Affected scope | 748 cases |
| Distribution | distributed in CA and OR. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0723-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Refreshe Mixed Berry Naturally Flavored Electrolyte Water, 12 bottles per cases, 1 L per bottle, sold under Safeway brand. The UPC 0 21130 24209 2.. Recalled by The Sweetwater Co., Inc.. Units affected: 748 cases.
Why was this product recalled? ▼
Sweetwater Company recalls Refreshe Mixed Berry Naturally Flavored Electrolyte Water (1 L size) due to elevated amount of non-fecal total Coliforms.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on December 11, 2013. Severity: Moderate. Recall number: F-0723-2014.
Where was the recalled product distributed? ▼
Distribution: distributed in CA and OR..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0723-2014) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported December 11, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.