Recall record at a glance
| Official record | F-0119-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | San Gennaro Foods, Inc. |
| Report date | Nov 15, 2017 |
| Recall initiation date | Oct 13, 2017 |
| Quantity | 3567 cases |
| Location | Kent, WA, United States |
Official product description
Italian Herb Polenta, Melissa's brand, Shelf stable, 12/16 oz packages UPC# 0-45255-11892-6 Ingredients: Water, Organic Cornmeal, Salt, Yeast Extract, Organic Tomato Powder, Organic Onion, Organic Parsley, Organic Oregano, Organic Granulated Onion, Tartaric Acid, Ascorbic Acid, Beta Carotene
Why the product was recalled
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
Distribution information
CA, CO, FL, GA, IL, IN, MD, ME, MI, NJ, NY, OR, PA, SC, TX, VA, WA, WI and Canada.
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken 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.