FDA recall record

Riviana International Ronzoni recall — FDA F-1965-2017

Undeclared egg. One lot Ronzoni Thin Spaghetti contained Ronzoni Egg Fettuccine.

Class Iclassification
F-1965-2017official record ID
Apr 26, 2017report date

Recall record at a glance

Official recordF-1965-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmRiviana International, Inc.
Report dateApr 26, 2017
Recall initiation dateMar 17, 2017
Quantity7320 units
LocationHouston, TX, United States

Official product description

Ronzoni(R) Thin Spaghetti, NO. 9, ENRICHED MACARONI PRODUCT, NET WT 16 OA (454g)., UPC 71300 00009

Why the product was recalled

Undeclared egg. One lot Ronzoni Thin Spaghetti contained Ronzoni Egg Fettuccine.

Distribution information

PA and FL

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.