Ronzoni Roasted Garlic Fettuccine recall
Recalled by EBRO North America dba New World Pasta · Harrisburg, PA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The firm initiated this recall as a precaution out of concern that the product contains an undeclared allergen soy . Even though the product may contain a very small amount of soy, it has been further processed so there is no detectable level of soy protein.
Undeclared allergen: Soy
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Ronzoni Roasted Garlic Fettuccine Net Wt. 12 OZ. Enriched Macaroni Product shelf-stable packed in blue paperboard box all codes
Quantity: 90,011 cases 12 units per case
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
all production codes and Best By dates
Where it was sold
California Connecticut Florida Massachusetts Minnesota Missouri New Jersey New York Pennsylvania Puerto Rico Texas Vermont
FDA's distribution note: CA CT FL MA MN MO NJ NY PA PR TX VT
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- EBRO North America dba New World Pasta
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 2, 2014
- In FDA report of
- Aug 20, 2014
- Terminated
- Apr 10, 2015
- FDA recall number
- F-2306-2014 · event 68682
- Official record
- FDA enforcement report search