Odwalla Superfood fruit smoothie 15.2 oz. (450mL) plastic bottle; Sold in 8 pack case Unit UPC: 000-14054-

Recall map → All recalls → F-1656-2018

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 The Coca-Cola Company · reported 2018-07-25

Terminated This recall has been closed out by the agency.

Reason for recall: There is the potential for a limited quantity of bottles to contain foreign matter in the form of tiny pieces of wire metal fragments.
Classification: Class II
Recall initiated: 2018-07-13
Reported by the agency: 2018-07-25
Closed out (terminated): 2018-08-23
Recalling firm: The Coca-Cola Company
Atlanta, GA
United States
This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
Distribution (the agency's own words): 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.
States we parsed from that text: AK AL AZ CA CO FL GA HI IA IL LA MA MD ME MI MN MO MS MT NC NM NV NY OH OR PA SC TX UT VA WA WI WY
The agency named these states. Parse method explicit_state_list, confidence high.
Food category: Beverages Produce (fruit & vegetables)derived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
Recall type: Voluntary: Firm initiated
Recall number: F-1656-2018

Verifying this record. Everything above is FDA's own record, reproduced. FDA publishes no web page for an individual enforcement report, so the only direct link is the machine-readable one:

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This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.