Salsa Dianne Recalls Classic Pesto Sauce Due to Undeclared Milk
Salsa Dianne recalls Classic Pesto Sauce (with a twist) because milk is not declared on the label, posing an allergy risk.
Use caution until it’s fixed
Classic Pesto Sauce (with a twist) is recalled because Parmesan cheese is declared but milk is not declared on label.
Contact the company
What happened, in plain English
Salsa Dianne is recalling its Classic Pesto Sauce (with a twist), net wt. 4 oz., because the label fails to declare milk as an ingredient. This omission poses a risk to individuals with milk allergies who may unknowingly consume the product. The recall was issued on April 7, 2016. Read more at govinfonow.com/recall/24891-salsa-dianne-recalls-classic-pesto-sauce-due-to-undeclared-milk.
Source Summary by GovInfoNow · govinfonow.com/recall/24891-salsa-dianne-recalls-classic-pesto-sauce-due-to-undeclared-milk · Updated October 11, 2026 · FDA enforcement record: FDA #F-1322-2016
Cite this page
“Salsa Dianne Recalls Classic Pesto Sauce Due to Undeclared Milk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/24891-salsa-dianne-recalls-classic-pesto-sauce-due-to-undeclared-milk. Based on FDA recall #F-1322-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1322-2016%22&limit=1).
Why it’s dangerous
The product contains milk, which is not listed on the ingredient label. For people with milk allergies, consuming this product could trigger an allergic reaction because they would be unaware of the presence of milk.
Who’s affected
Consumers in Oregon who purchased Classic Pesto Sauce (with a twist) between production and April 30, 2016 are affected. Individuals with milk allergies or sensitivities are at the highest risk due to the undeclared ingredient.
How to tell if you have this one
Check for Classic Pesto Sauce (with a twist) in round Styrofoam containers with translucent plastic lids. Look for UPC 8 20103 77214 3 and a 'best if used by' date of 4/30/2016. The label should list 'Made & Packaged by Dianne's Kitchen, Union, Oregon 97883'.
- Brand
Salsa Dianne- Product
Classic Pesto Sauce (with a twist), net wt. 4 oz. (113 g). Product is packaged in a round Styrofoam containers with- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
distributed in Oregon
| Recall number | Product, codes & lots |
|---|---|
| F-1322-2016 | Classic Pesto Sauce (with a twist), net wt. 4 oz. (113 g). Product is packaged in a round Styrofoam containers with translucent plastic lid. The UPC is 8 20103 77214 3. The product is labeled in parts: "***Classic Pesto (with a twist)***INGREDIENTS: Olive Oil, Brazil nuts, Garlic, Parmesan cheese, Basil, Onion***Made & Packaged by Dianne's Kitchen***Union, Oregon 97883***".; best if used (or frozen) by 4/30/2016 |
| F-1323-2016 | Lemon Pesto Sauce, net wt. 4 oz. (113 g). Product is packaged in a round Styrofoam containers with translucent plastic lid. The UPC is 8 20103 77213 6. The product is labeled in parts: "***Lemon Pesto***INGREDIENTS: Olive Oil, Lemon, Almonds, Garlic, Parmesan cheese, Cilantro, Onion***Made & Packaged by Dianne's Kitchen***Union, Oregon 97883***".; best if used (or frozen) by 4/30/2016 |
What to do — step by step
Check Your Product
Verify if you have the recalled Classic Pesto Sauce by checking the UPC and packaging details.
Contact Manufacturer
Since no specific remedy is provided in the record, contact Salsa Dianne for further instructions on returns or refunds.
Where it went and when
Where it was distributed
Distributed in Oregon.
FDA distribution: “distributed in Oregon” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Oregon.
Recall timeline
FDA terminated this recall 47 days 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-1322-2016 (April 7, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1322-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.