L-Nutra Inc Recall: Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.
United States
OngoingClass II
- Company
- L-Nutra Inc
- Product
- Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47…
- Recall date
- August 7, 2026
- Source
- FDA
Reason for recall
Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | 50040360530 | 8,529 jars | Lot code: L2755 Expiration: 02 Jan 2027 |
Distribution
- Product is sold exclusively from the recalling firm's online website nationwide.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-1335-2026
- Event ID
- 99675
- Status
- Ongoing
- Classification
- Class II
- Company
- L-Nutra Inc
- 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
- Quantity
- 8,529 jars
- Reason
- Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.
- Recall initiation date
- August 7, 2026
- Report date
- September 16, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Product is sold exclusively from the recalling firm's online website nationwide.
- UPC, lot, and code information
- UPC 50040360530; Lot code: L2755 Expiration: 02 Jan 2027
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: L-Nutra Inc
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
