Lower riskFood recall · FDA · Published August 7, 2026
L-Nutra Prolon Almond Cocoa Spread Recall: Undeclared Tree Nuts Hazard
L-Nutra recalls Prolon Everyday Apulian Almond & Cocoa Spread due to undeclared tree nuts (hazelnut, cashew, pistachio) in glass jars with white label and gold closure.
“L-Nutra Prolon Almond Cocoa Spread Recall: Undeclared Tree Nuts Hazard.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/994916-l-nutra-prolon-almond-cocoa-spread-recall-undeclared-tree-nuts. Based on FDA recall #H-1335-2026.
The FDA announced on August 7, 2026, that L-Nutra Inc is recalling Prolon Everyday Apulian Almond & Cocoa Spread due to undeclared tree nut allergens. The product may contain hazelnut, cashew, and pistachio.
How to tell if you have it
Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ.
UPC: 50040360530
Lot code: L2755
Expiration: 02 Jan 2027
The hazard
The spread contains undeclared tree nuts, specifically hazelnut, cashew, and pistachio. These allergens pose a risk to consumers with allergies.
Context
GovInfoNow's records show that Fayus issued a recall for OLA-OLA Pounded Groundnuts on June 19, 2026, due to undeclared peanuts. Wilco Peanut Co recalled Raw Shelled Peanuts on May 18, 2026, citing an undeclared tree nut allergen risk. Bazzini issued a recall for Dark Chocolate Coconut Almond Bites on May 23, 2026, due to undeclared peanuts.
How to tell if you have this one
Check for glass jars with white labels and gold screw-on closures. The product has a UPC of 50040360530 and lot code L2755, expiring January 2027.
Brand
L-Nutra
Product
Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ. Product packaged in glass jar with white label and gold
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for glass jars with white labels and gold screw-on closures.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Product is sold exclusively from the recalling firm's online website nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 40 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-1335-2026 (August 7, 2026)
Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.