Class IIOngoingVoluntary: Firm initiated
L-Nutra Inc: food recall H-1335-2026
L-Nutra Inc of Los Angeles, CA recalled Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ. Product packaged in glass jar with white label and… Reason: Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio. The FDA listed it as Class II in its Enforcement Report dated Sep 16, 2026; distribution: nationwide.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 8,529 jars
- Reason for recall
- Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.
- Codes, lots and dates on the package
- Lot code: L2755 Expiration: 02 Jan 2027
- Distribution pattern
- Product is sold exclusively from the recalling firm's online website nationwide.
- Recalling firm
- L-Nutra Inc, Los Angeles, CA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Aug 7, 2026 |
| Classified by the FDA | Sep 10, 2026 |
| Published in the Enforcement Report | Sep 16, 2026 |
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1335-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.