Recall record at a glance
| Official record | F-1656-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | The Coca-Cola Company |
| Report date | Jul 25, 2018 |
| Recall initiation date | Jul 13, 2018 |
| Quantity | 14,870 cases |
| Location | Atlanta, GA, United States |
Official product description
Odwalla Superfood fruit smoothie 15.2 oz. (450mL) plastic bottle; Sold in 8 pack case Unit UPC: 000-14054-06405-5 Odwalla Life Food- Canada only - Unit UPC: 000-14054-03125-5 Ingredients: Apple Juice from concentrate, peach and mango purees from concentrate, banana puree, less than 1% OF, Spirulina, natural flavors, lemon juice concentrate (for tartness) vitamin C (ascorbic acid) kale, wheat grass, barley grass, wheat sprouts, Jerusalem artichoke, Nova Scotia dulse Pectin and gellan gum. Contains Wheat. Distributed by Odwalla Inc., San Leandro, CA 94577 Pasteurized. Must be refrigerated
Why the product was recalled
There is the potential for a limited quantity of bottles to contain foreign matter in the form of tiny pieces of wire metal fragments.
Distribution information
Alaska, Alabama, Arizona, California, Colorado, Florida, Georgia, Hawaii, Iowa, Illinois, Louisiana, Massachusetts, Maine, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, New Mexico, Nevada, New York, Ohio, Oregon, Pennsylvania, South Carolina, Texas, Utah, Virginia, Washington, Wisconsin and Wyoming and Canada.
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: Letter.
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.
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