Class IITerminated in FDA datasetRecall initiated Jul 13, 2018

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

Why it was recalled

Possible metal fragments

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 23, 2018.

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Compare the exact product and package details with the label you have.

ProductOdwalla 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

Package size15.2 oz

FDA code information

AUG 3118 AS; SEP 0218 AS; SEP 0318 AS; Canadian distribution: SEP 0218 AS.

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Full FDA record and distribution details

Original 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

Original FDA recall reason

There is the potential for a limited quantity of bottles to contain foreign matter in the form of tiny pieces of wire metal fragments.

Recall details

Recall number: F-1656-2018
Event ID: 80532
FDA status: Terminated
Initiated: Jul 13, 2018
Reported: Jul 25, 2018
Classified: Jul 19, 2018
Terminated: Aug 23, 2018
Quantity: 14,870 cases
Location: Atlanta, GA, United States
Initiation type: Voluntary: Firm initiated
Notification: Letter

Where it was distributed

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.

FDA source record · F-1656-2018

Data updated September 16, 2026. View official FDA data ↗

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