Naturefood 2010 NutiLight Protein Spread Recall: Listeria Risk
Naturefood 2010 recalls NutiLight Protein + Pistachio Spread due to potential Listeria monocytogenes contamination. Consumers should check product codes and follow official instructions.
Recall notice
Listeria monocytogenes.
Contact the company
What happened, in plain English
Naturefood 2010 is recalling NutiLight Protein + Pistachio Spread because it may contain Listeria monocytogenes, a bacteria that can cause serious illness. This recall affects products sold in the U.S. with the code PSP 7329. Read more at govinfonow.com/recall/20821-naturefood-2010-nutilight-protein-spread-recall-listeria-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/20821-naturefood-2010-nutilight-protein-spread-recall-listeria-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2946-2017
Cite this page
“Naturefood 2010 NutiLight Protein Spread Recall: Listeria Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/20821-naturefood-2010-nutilight-protein-spread-recall-listeria-risk. Based on FDA recall #F-2946-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2946-2017%22&limit=1).
Why it’s dangerous
Listeria monocytogenes is a bacteria that can cause serious infections, especially in pregnant women, newborns, and people with weakened immune systems. It can lead to fever, muscle aches, and in severe cases, life-threatening complications.
Who’s affected
People who own or use the recalled NutiLight Protein + Pistachio Spread product are affected. Those with weakened immune systems are at higher risk of serious illness from Listeria.
How to tell if you have this one
Check for the product code PSP 7329 on the label. The product is sold in the U.S. with a net weight of 11oz (312gr).
- Brand
Naturefood 2010- Category
Food
What to do — step by step
Check Product Code
Look for the code PSP 7329 on the label to confirm if your product is recalled.
How this recall unfolded
Recall timeline
FDA terminated this recall 14 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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 #F-2946-2017 (June 13, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2946-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.