Class IIITerminatedVoluntary: Firm initiated
Refresqueria Estrella Inc.: food recall H-0913-2026
Refresqueria Estrella Inc. of Bayamon, PR recalled ESTRELLA, Bebida de Parcha (Passion Fruit Drink), multiple sizes, 14 OZ.FL. (413 ML), 64 OZ.FL (1,920mL), 120 OZ.FL.… Reason: Undeclared FD&C Red 40. The FDA listed it as Class III in its Enforcement Report dated Jun 17, 2026; distribution: Puerto Rico.
Record status as published: Terminated (terminated Aug 18, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- ESTRELLA, Bebida de Parcha (Passion Fruit Drink), multiple sizes, 14 OZ.FL. (413 ML), 64 OZ.FL (1,920mL), 120 OZ.FL. (3.54LT.) 14 OZ.FL Plastic Bottles packed in cases of 25 bottles. KEEP REFRIGIRATED.
- Product quantity
- Total: 2,111---14 oz-1,291, 64 oz-114 and 120 oz -706
- Reason for recall
- Undeclared FD&C Red 40
- Codes, lots and dates on the package
- May Production Lot Code:12426, 13126, 13426. 4/8/2026 Expiration Date: 4/8/2026, 5/8/2026, 6/8/2026, 11/8/2026, 11/8/2026, 14-08-2026, 14-08-2026 April Production Lot Code: 9226, 9626, 9826, 9926, 10326, 10626, 11026, 11126, 11326, 11826, 11926, 12026 Expiration Date:2/7/2026, 6/7/2026, 8/7/2026, 9/7/2026, 13-07-2026, 16-07-2026, 16-07-2026, 20-07-2026, 21-07-2026, 22-07-2026, 23-07-2026, 23-07-2026, 28-07-2026, 29-07-2026 30-07-2026 March Production Lot Code:6126, 6426, 7026, 9926, 8326, 8226, 8626, 9026 Expiration Date: 2/6/2026, 5/6/2026, 11/6/2026, 20-06-2026, 23-06-2026, 24-06-2026, 27-06-2026, 30-06-2026
- Distribution pattern
- Puerto Rico distribution only.
- Recalling firm
- Refresqueria Estrella Inc., Bayamon, PR
- Classification
- Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 19, 2026 |
| Classified by the FDA | Jun 9, 2026 |
| Published in the Enforcement Report | Jun 17, 2026 |
| Terminated | Aug 18, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0913-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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