CLASS III ONGOING Food recall · Reported 21 Oct 2026 · FDA Enforcement Report
Pur Aqua Sparkling Frost Cherry Limeade recalled
Refresco Beverages US is recalling Pur Aqua Sparkling Frost Cherry Limeade, distributed in Florida. The recall was initiated on 7 Oct 2026 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0095-2027
- FDA event ID
- 100096
- Recalling firm
- Refresco Beverages US, Tampa, FL
- Brand
- Pur Aqua
- Classification
- Class III
- Status
- Ongoing
- Recall initiated
- 7 Oct 2026
- FDA classified
- 15 Oct 2026
- Reported
- 21 Oct 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Allergens
- Product category
- Alcohol
Timeline
| 7 Oct 2026 | Recall initiated by company | |
| 15 Oct 2026 | Classified by FDA | +8 days |
| 21 Oct 2026 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
May contain undeclared aspartame.
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Pur Aqua Sparkling Frost Cherry Limeade 17 oz., UPC: 4099100167023
Where it was distributed
Florida with further downstream distribution to retail stores
Questions about this recall
Why was it recalled?
May contain undeclared aspartame.
Which lots are affected?
Best if use by: 032327 TA
Where was it sold?
Florida with further downstream distribution to retail stores
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 27 Oct 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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