Recall record at a glance
| Official record | F-2739-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | San Francisco Spice Company, Inc. |
| Report date | Jul 1, 2015 |
| Recall initiation date | Jun 3, 2015 |
| Quantity | 13,908 individual units |
| Location | South San Francisco, CA, United States |
Official product description
Eating Right Black Bean Soup; 1.3 oz paper container. Dried soup to which consumer adds hot water. USPC: 79893-80026; Ingredients: Ingredients: Black Beans*, Vegetables* (Tomato, Potato, Corn, Peppers, Garlic), Natural Flavor (Yeast Extract, Maltodextrin, Sunflower Oil, Silicon Dioxide, Natural Flavor), Spice, Salt, Oregano.* *Dried Cases of Eating Right Spicy Thai Soup (12 x 1.3 oz. containers per case), USPC: 79893-80030. Ingredients: Please note that Spicy Thai Noodle has noodles in a cup and then a sealed flavor packet inside the cup which consumers must open and pour out. Ingredients: Noodles* (Durum Semolina Wheat Flour, Niacin, Ferrous Sulfate (Iron), Thiamine Mononitrate, Riboflavin, Folic Acid), Vegetables* (White Onion, Green Onion, Garlic, Bell Pepper, Shallots), Natural Flavors (Yeast Extract, Tapioca Maltodextrin, Chicken Fat, Dextrose, Salt, Potassium Chloride, Anchovy (Fish), Lactic Acid, Glycerine, Silicon Dioxide), Dried Cane Syrup, Soy Sauce* (Soybeans, Wheat), Sesame (Seeds and Oil), Spices (Including Mild Chilies, Lemongrass, Ginger, Black Pepper, Cumin, Cayenne, Turmeric), Lime*, Cilantro*, Basil*, Citric Acid, Guar and Xanthan Gum, Tamarind*, Extract of Paprika. *Dried Eating Right is a SafeTway brand name and is only sold in Safeway stores and their subsidiaries of Vons. Mfg for Safeway by San Francisco Spice Co., So. San Francisco, CA.
Why the product was recalled
Some containers or Eating Right Black Bean Coup may contain Eating Right Spicy Thai Noodle inside.
Distribution information
CA, OR, WA, AK, ID. NV, HI
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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.