Del Monte Park Street Deli Hummus Recall: Undeclared Peanut Butter Hazard
Del Monte recalls Park Street Deli Hummus products due to undeclared peanut butter. Consumers should check for lot number 09129101 and contact Del Monte for details.
Recall notice
Undeclared peanut butter
Contact the company
What happened, in plain English
Del Monte is recalling Park Street Deli hummus products that contain undeclared peanut butter. This poses a risk for people with peanut allergies who may react to the hidden peanut content. Read more at govinfonow.com/recall/17457-del-monte-park-street-deli-hummus-recall-undeclared-peanut-butter.
Source Summary by GovInfoNow · govinfonow.com/recall/17457-del-monte-park-street-deli-hummus-recall-undeclared-peanut-butter · Updated October 5, 2026 · FDA enforcement record: FDA #F-1457-2019
Cite this page
“Del Monte Park Street Deli Hummus Recall: Undeclared Peanut Butter Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17457-del-monte-park-street-deli-hummus-recall-undeclared-peanut-butter. Based on FDA recall #F-1457-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1457-2019%22&limit=1).
Why it’s dangerous
The hummus products contain peanut butter that was not declared on the label. This means people with peanut allergies could have a severe allergic reaction if they consume the product.
Who’s affected
People with peanut allergies are at risk from this undeclared peanut butter in the hummus products. Anyone who purchased these items from the recall lot should check if they have the product.
How to tell if you have this one
Check for the lot number 09129101 on the packaging of Park Street Deli Hummus products. The products include Classic Hummus, Carrots & Celery, and are sold in 5 oz (142g) containers.
- Brand
Del Monte- Category
Food
What to do — step by step
Check Product Label
Look for the lot number 09129101 on the packaging of Park Street Deli Hummus products.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “NY, PA, IL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, New York, Pennsylvania.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- 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-1457-2019 (May 20, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1457-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.