El David Gelee, Bonbons with fruits Soft & Juicy, 400g. Packaged in decorated paperboard box and covered entirely in tra
Summary
The FDA issued a Class II for El David Gelee, Bonbons with fruits Soft & Juicy, 400g. Packaged in decorated pa by Alb-USA Enterprises Inc. Reason: Undeclared colors (FD&C Yellow 5 and FD&C Red 40)..
Details
Source
Food Recall
External ID
H-1110-2026
Action Date
2026-07-01
Status
Ongoing
Category
food
Product Description
El David Gelee, Bonbons with fruits Soft & Juicy, 400g. Packaged in decorated paperboard box and covered entirely in transparent, flexible plastic wrap. (20 bonbon pieces per 400g box). UPC 5304000050757
Lot/Code Info: Expiration Date(s): 12.05.2027
Quantity Affected: 15 (400g) boxed units (20 pieces/box)
Reason for Recall
Undeclared colors (FD&C Yellow 5 and FD&C Red 40).
Distribution
NY, NJ
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-21
Company
Bronx, NY
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 58 food recalls issued in the same week, part of 92 food-related FDA actions this month.
Alb-USA Enterprises Inc has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Alb-USA Enterprises Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Alb-USA Enterprises Inc have FDA actions?
Alb-USA Enterprises Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1110-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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