ESTRELLA Bebida de Parcha recall
Recalled by Refresqueria Estrella Inc. · Bayamon, PR, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Undeclared FD&C Red 40
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
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.
Quantity: Total: 2,111---14 oz-1,291, 64 oz-114 and 120 oz -706
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your 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
Where it was sold
Puerto Rico
FDA's distribution note: Puerto Rico distribution only.
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Refresqueria Estrella Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 19, 2026
- In FDA report of
- Jun 17, 2026
- Terminated
- Aug 18, 2026
- FDA recall number
- H-0913-2026 · event 99037
- Official record
- FDA enforcement report search