Recall Register

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

Class III FDA enforcement event 100096. Recall start date: . Status in the FDA record: Ongoing.

Reason for recall, in the words of FDA

May contain undeclared aspartame.

Class III, in the words of FDA

a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences

Refresco Beverages US Inc started this food recall on 7 Oct 2026. The firm address in the FDA record is in Tampa, FL. FDA put the recall in Class III. FDA event 100096 has 1 product record. The first FDA enforcement report date is 21 Oct 2026. The record gives the status Ongoing. 108 of the 339 food events that started in 2026 have more product records. The median food event of 2026 has 1 product record.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Florida with further downstream distribution to retail stores

Recalling firm

Refresco Beverages US Inc, Tampa, FL.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 100096: product records
Recall numberProductQuantityClassStatusReport date
H-0095-2027Pur Aqua Sparkling Frost Cherry Limeade 17 oz., UPC: 40991001670232100 unitsClass IIIOngoing21 Oct 2026

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class III: The lowest of the three FDA recall classes.

The event in context

Food events that started in 2026
339
Share of these events in Class III
6%
Product records in this event
1Median of the firm: 1
Events of the firm on the register
4

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 100096. https://recallregister.com/fda/iii/100096/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
27 Oct 2026
Newest FDA report date on the register
21 Oct 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Florida with further downstream distribution to retail stores
What quantity of product is in FDA event 100096?
The FDA record gives this quantity: 2100 units
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2026 have the same class?
6% of the 339 food events that started in 2026 are in Class III.