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RECALL RECORD — CLASS IIRecall closedF-0722-2014/FDA enforcement
The Sweetwater Co., INC.·Food·Oct 24, 2013

Refreshe Lime Naturally Flavored Electrolyte Water, 12 Bottles Per Cases, 1 L Per Bottle, Sold…

What you need to know

Class II

  • What happened

    Sweetwater Company recalls Refreshe Lime Naturally Flavored Electrolyte Water (1 L size) due to elevated amount of non-fecal total Coliforms.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAIN, CA, ORMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameThe Sweetwater Co., INC.
Recalling firmThe Sweetwater Co., INC.Culver, OR, United States
UPC / barcodes
0 21130 24208 5
Lot / date codes
  • 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.
Distribution area
INCAOR

distributed in CA and OR.

United States

Quantity affected680 cases
Recall initiationFDA report date: December 11, 2013
FDA recall numberF-0722-2014

Beyond the headline

The recall, in context

The Sweetwater Co., INC. initiated this food recall on October 24, 2013. The FDA enforcement report states: Sweetwater Company recalls Refreshe Lime Naturally Flavored Electrolyte Water (1 L size) due to elevated amount of non-fecal total Coliforms. The FDA report lists distribution as: distributed in CA and OR.

The FDA enforcement report describes the reason as: Sweetwater Company recalls Refreshe Lime Naturally Flavored Electrolyte Water (1 L size) due to elevated amount of non-fecal total Coliforms.

Refreshe Lime Naturally Flavored Electrolyte Water, 12 Bottles Per Cases, 1 L Per Bottle, Sold… was made or distributed by The Sweetwater Co., INC. in Culver, OR, United States. This page reflects FDA report F-0722-2014, dated December 11, 2013.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Refreshe Lime Naturally Flavored Electrolyte Water, 12 Bottles Per Cases, 1 L Per Bottle, Sold… recall?

The Sweetwater Co., INC. recalled Refreshe Lime Naturally Flavored Electrolyte Water, 12 Bottles Per Cases, 1 L Per Bottle, Sold… in an FDA Class II enforcement action reported as F-0722-2014. Sweetwater Company recalls Refreshe Lime Naturally Flavored Electrolyte Water (1 L size) due to elevated amount of non-fecal total Coliforms.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the The Sweetwater Co., INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0722-2014. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by The Sweetwater Co., INC.

View brand
Class III·

The Sweetwater Co., INC.

Lime Flavored Electrolyte Bottled Water, Sold Under Brand Refreshe

Lime Flavored Electrolyte bottled Water is recalled due to high total coliform testing results.

INFood
Class III·

The Sweetwater Co., INC.

Lemon Flavored Electrolyte Bottled Water, Sold Under Brand Hyvee, Raleys' Purely Made, …

Lemon Flavored Electrolyte water is recalled due to high total coliform testing results.

INFood

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.