Deano's Pasta food recall: Deano's Pasta
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 99966
- Recall initiated
- Sep 23, 2026
- Classified by FDA
- Oct 15, 2026
- Posted in Enforcement Report
- Oct 21, 2026
- Recalling firm
- DEANO'S PASTA
- Firm location
- Somerville, MA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Undeclared Lobster
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Sep 23, 2026. FDA classified it 22 days later, on Oct 15, 2026. Distribution reported by FDA: MA, NH
Recalled products (1)
H-0092-2027 Class I Ongoing
Deano's Pasta; Pear and Pecorino Triangoli Ravioli, 1lb.; Ingredients: Dough: Semolina (Wheat, Niacin, Thiamine, Mononitrate, Riboflavin, Folic Acid), Water, Fresh Eggs, Salt. Filling: Pears, Ricotta (Whey, Cream, Milk), Pecorino Cheese (Milk, Cultures, Salt, Enzymes), Breadcrumbs (Wheat Flour, Cane Sugar, Yeast, Salt), Brandy, Dark Brown Sugar, Salt, Black Pepper.; CONTAINS: WHEAT, MILK, EGG ingredients; MAY CONTAIN OTHER ALLERGENS; KEEP FROZEN
Codes / lots: lot codes 090126126, 082526126,081826126, and 073126126
Quantity: 78lbs
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 99966
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.