United States
TerminatedClass II
Recall of products manufactured with vegetables from McCain Foods USA and currently under recall for potential Salmonella and/or Listeria Monocytogenes contamination
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Cadence Gourmet Cauliflower & Cheese Net Weight: 10 lbs. (4.4 kg) / cs UPC: 00851124006375 Ingredients: Cauliflower, B¿chamel Sauce (Milk, Cultured Cream, Vegetable Broth [Water, sauteed Vegetables {carrots, celery, onions, tomatoes}, Salt, Yeast Extract, Dried Onion and Garlic, Potato Flakes and Natural Flavor] Butter [Pasteurized cream, salt] Corn Starch, Garlic Powder, Black Pepper, Paprika, Monterey Jack Cheese (Pasteurized Milk, Cheese Cultures, Salt, Enzymes, Powdered Cellulose {Added to prevent caking], Natamycin {A Natural Mold inhibitor] Parmesan Cheese (Pasteurized Skim Milk, Cheese Cultures, Salt, Enzymes, Powdered Potato Starch and corn starch {added to prevent caking], Natamycin {a Natural Mold Inhibitor], Bacon (Cured pork with Water, salt, smoke flavoring, Sodium Phosphate, Sodium Erythorbate, Sodium Nitrate, May contain Sugar, Brown Sugar, Potassium Chloride) and Basil Contains: Milk Keep Frozen. Manufactured by: Cadence Gourmet, Corona, CA 92880 | 00851124006375 | 5650 lb | Product SS00033 Lot/Batch numbers: 173231 173421 180031 |
This recall shares FDA event ID 81438 with 3 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: February 20, 2019Historical recordClass II
FDA Recall United States TerminatedTerminated: February 20, 2019Historical recordClass II
FDA Recall United States TerminatedTerminated: February 20, 2019Historical recordClass II
Responsible company: Cadence Gourmet LLC
FDA Recall United States TerminatedTerminated: February 20, 2019Historical recordClass II
FDA Recall United States TerminatedTerminated: February 20, 2019Historical recordClass II
FDA Recall United States TerminatedTerminated: February 20, 2019Historical recordClass II
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 |
|---|---|
| Utah | 1 |
| California | 1 |
| Maryland | 1 |
| Texas | 1 |
| Kansas | 1 |
| Illinois | 1 |
| Georgia | 1 |
| Florida | 1 |
| Washington | 1 |
| New Mexico | 1 |
| Colorado | 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.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
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.
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
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This record is preserved as published by FDA, as of February 20, 2019.
Status as reported: Terminated.
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