Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ. Product packaged in glass jar with white label and gold
Summary
The FDA issued a Class II for Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ. Product packaged by L-Nutra Inc. Reason: Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio..
Details
Source
Food Recall
External ID
H-1335-2026
Action Date
2026-09-16
Status
Ongoing
Category
food
Product Description
Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ. Product packaged in glass jar with white label and gold screw on closure. UPC: 50040360530
Lot/Code Info: Lot code: L2755 Expiration: 02 Jan 2027
Quantity Affected: 8,529 jars
Reason for Recall
Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.
Distribution
Product is sold exclusively from the recalling firm's online website nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-08-07
Company
Los Angeles, CA
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 24 food recalls issued in the same week, part of 82 food-related FDA actions this month.
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 (L-Nutra Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does L-Nutra Inc have FDA actions?
This is the only FDA action we have on record for L-Nutra Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1335-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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