FDA Recall United States Terminated Historical recordClass II
Riviana International, Inc
- Product
- Mahatma Broccoli & Cheese Rice; 4 oz. net weight (UPC 17400-…
- Published
- March 1, 2017
- Distribution
- Multiple states
Riviana International, Inc Recall: Undeclared egg. One lot Ronzoni Thin Spaghetti contained Ronzoni Egg Fettuccine.
United States
TerminatedClass I
- Company
- Riviana International, Inc
- Product
- Ronzoni(R) Thin Spaghetti, NO. 9, ENRICHED MACARONI PRODUCT,…
- Recall date
- March 17, 2017
- Terminated
- August 22, 2017
- Source
- FDA
Reason for recall
Undeclared egg. One lot Ronzoni Thin Spaghetti contained Ronzoni Egg Fettuccine.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Ronzoni(R) Thin Spaghetti, NO. 9, ENRICHED MACARONI PRODUCT, NET WT 16 OA (454g)., UPC 71300 00009 | Not published in this source record | 7320 units | Code: JAN 20 19 K |
Distribution
- PA and FL
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1965-2017
- Event ID
- 76788
- Status
- Terminated
- Classification
- Class I
- Company
- Riviana International, Inc
- Product description
- Ronzoni(R) Thin Spaghetti, NO. 9, ENRICHED MACARONI PRODUCT, NET WT 16 OA (454g)., UPC 71300 00009
- Quantity
- 7320 units
- Reason
- Undeclared egg. One lot Ronzoni Thin Spaghetti contained Ronzoni Egg Fettuccine.
- Recall initiation date
- March 17, 2017
- Report date
- April 26, 2017
- Classification date
- Not published in this source record
- Termination date
- August 22, 2017
- Distribution pattern
- PA and FL
- UPC, lot, and code information
- Code: JAN 20 19 K
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Riviana International, Inc
Other recalls from Riviana International, Inc
FDA Recall United States Terminated Historical recordClass II
Riviana International, Inc
- Product
- (a) Mahatma(R) Saffron YELLOW seasonings & LONG GRAIN RICE;…
- Published
- March 1, 2017
- Distribution
- Multiple states
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Pennsylvania | 1 |
| Florida | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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