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Recalls Watch

FDA recall 100096: Refresco Beverages US Inc: Pur Aqua Sparkling Frost Cherry Limeade 17 oz.

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FDARecall 100096Food

What to do

The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Note from Recalls Watch, not agency text.

Read the official notice on accessdata.fda.gov (opens in a new tab)

Hazard

Why it was recalled

May contain undeclared aspartame.
Text from FDA, unedited.

FDA classification: Class III. Use is not likely to cause adverse health consequences. Status: Ongoing.

Is it yours? Products and codes

Type the lot, batch, date code, model number or UPC printed on the product. It is compared here, in your browser, with the codes this notice lists. The code is also added to the page address (?lot=…), so a copied link or result carries it.

General information on recalls from the agency: U.S. Food and Drug Administration (opens in a new tab).

  • Pur Aqua Sparkling Frost Cherry Limeade 17 oz., UPC: 4099100167023

    Lot or code
    Best if use by: 032327 TA
    FDA recall number
    H-0095-2027
    Quantity
    2100 units

Distribution (FDA): Florida with further downstream distribution to retail stores

About this record

Issued by
U.S. Food and Drug Administration
Firm
Refresco Beverages US Inc
Title
Composed by Recalls Watch from fields of the record; FDA records have no title.

If someone was hurt or swallowed something: call 911, or Poison Help at 1-800-222-1222.

Directory and lookup links

Check all notices from this recalling firm in the directory of recalls by brand and manufacturer. Browse more food recalls, or check another notice by its number in the recall number lookup.

About this recall

What is the hazard?

FDA states: “May contain undeclared aspartame.”

What should I do if I have this product?

The FDA record of this recall has no instruction for consumers. Compare the lot codes on the notice with your product and follow the notice of the firm. The official report is linked on this page.

How do I know if my product is included?

Compare the lot or code printed on your product with the codes FDA lists on this notice, product by product.

How does the code check on this page work?

You type the lot, batch, date code, model number or UPC from your package and the page compares it, in your browser, with the codes FDA lists on this notice. It reports a match, a possible match (your code is part of a longer listed code) or no match. It only compares text: a notice that describes products by dates, sizes or “all lots” cannot be compared, so “no match” does not clear a product. The comparison runs in your browser and the page does not send the code anywhere, but the code is added to the page address (?lot=…): a link you copy, share or bookmark carries it, and whoever opens that link requests that address from this site.

When was this recall published?

FDA published recall 100096 on October 21, 2026.

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