BLM Products Priano Rosso Pesto Sauce Recall: Undeclared Allergens Egg and Milk
BLM Products recalls Priano Rosso Pesto Sauce (6.7oz glass jars) due to undeclared allergens egg and milk. Consumers should check lot codes from July 2019 to September 2019 for affected products.
Lower-risk recall
BLM Prod.-und Vertriebsges.mbH & Co. KG has initiated a voluntary recall of Priano Rosso Pesto Sauce, 6.7 oz. packaged in glass jars due to undeclared allergens egg and milk.
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What happened, in plain English
BLM Products is recalling Priano Rosso Pesto Sauce in 6.7oz glass jars because it contains undeclared allergens: egg and milk. This poses a risk for people with allergies to these ingredients, as they may not be aware the sauce contains them. Read more at govinfonow.com/recall/19126-blm-products-priano-rosso-pesto-sauce-recall-undeclared-allergens-egg.
Source Summary by GovInfoNow · govinfonow.com/recall/19126-blm-products-priano-rosso-pesto-sauce-recall-undeclared-allergens-egg · Updated October 7, 2026 · FDA enforcement record: FDA #F-1548-2018
Cite this page
“BLM Products Priano Rosso Pesto Sauce Recall: Undeclared Allergens Egg and Milk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19126-blm-products-priano-rosso-pesto-sauce-recall-undeclared-allergens-egg. Based on FDA recall #F-1548-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1548-2018%22&limit=1).
Why it’s dangerous
The sauce contains undeclared allergens (egg and milk) that could cause allergic reactions in sensitive individuals. Since the allergens are not listed on the label, people with allergies might unknowingly consume them.
Who’s affected
People with egg or milk allergies who consume the recalled sauce may experience allergic reactions. The recall affects consumers who bought the sauce between July and September 2019.
How to tell if you have this one
Check for glass jars labeled 'Priano Rosso Pesto Sauce, 6.7oz' with lot codes from July 2019 to September 2019 as listed in the recall notice.
- Brand
BLM Products- Category
Food
What to do — step by step
Check Product Lot Code
Look for lot codes such as LA 016, LA 017, LA 052, LA 053, LA 085, LAB 312, or LAB 324-325 on the jar's label.
Where it went and when
Where it was distributed
Distributed in 30 states and D.C..
FDA distribution: “Domestic only: Arkansas, California, Connecticut, District of Columbia, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Maryland, Massachusetts, Michigan, Missouri, North Carolina, Nebraska, New Hampshire, New…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arkansas, California, Connecticut, Delaware, District of Columbia, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Maryland, Massachusetts, Michigan, Missouri, Nebraska, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Vermont, Virginia, West Virginia.
Recall timeline
FDA terminated this recall 5 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.
Questions people ask
Do I need to stop using this sauce?
No immediate action is required beyond checking the lot code. If you have the affected lot code, you should avoid using it due to the allergen risk.
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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-1548-2018 (May 15, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1548-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.