ESTRELLA, Bebida de Parcha (Passion Fruit Drink), multiple sizes, 14 OZ.FL. (413 ML), 64 OZ.FL (1,920mL), 120 OZ.FL. (3
Summary
The FDA issued a Class III for ESTRELLA, Bebida de Parcha (Passion Fruit Drink), multiple sizes, 14 OZ.FL. (41 by Refresqueria Estrella Inc.. Reason: Undeclared FD&C Red 40.
Details
Source
Food Recall
External ID
H-0913-2026
Action Date
2026-06-17
Status
Ongoing
Category
food
Product Description
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.
Lot/Code Info: 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
Quantity Affected: Total: 2,111---14 oz-1,291, 64 oz-114 and 120 oz -706
Reason for Recall
Undeclared FD&C Red 40
Distribution
Puerto Rico distribution only.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-19
Company
Bayamon, PR
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 191 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Refresqueria Estrella Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Refresqueria Estrella Inc. have FDA actions?
This is the only FDA action we have on record for Refresqueria Estrella Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0913-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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