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Class II: temporary or reversible health riskTerminated

The Coca-Cola Odwalla Superfood fruit smoothie 15 Recall

Odwalla Superfood fruit smoothie 15

The Coca-Cola Company · Atlanta, GA

Risk level
Class II
Reported by FDA
Jul 25, 2018
Recall ID
F-1656-2018
Check your lot numberHow we source this data

Summary

The Coca-Cola recalled Odwalla Superfood fruit smoothie 15 starting Jul 13, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1656-2018 on Jul 25, 2018. 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. Status: Terminated.

Why it 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.

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

Lot numbers, UPCs & expiration codes

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

Where it was sold

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.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1656-2018
Classification
Class II
Status
Terminated
Recall initiated
Jul 13, 2018
FDA report date
Jul 25, 2018
Quantity
14,870 cases
Recall type
Voluntary: Firm initiated
Recalling firm
The Coca-Cola Company

Original FDA data

Every field from FDA enforcement report F-1656-2018, exactly as published.

Show all FDA fields
City
Atlanta
State
GA
Status
Terminated
Country
United States
Event ID
80532
Address
Atlanta Office Complex
Address (line 2)
1 Coca Cola Plz NW
Code information
AUG 3118 AS; SEP 0218 AS; SEP 0318 AS; Canadian distribution: SEP 0218 AS.
Postal code
30313-2420
Report date
Jul 25, 2018
Product type
Food
Recall number
F-1656-2018
Classification
Class II
Recalling firm
The Coca-Cola Company
Product quantity
14,870 cases
Termination date
Aug 23, 2018
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.
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
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.
Recall initiation date
Jul 13, 2018
Initial firm notification
Letter
Center classification date
Jul 19, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1656-2018, published Jul 25, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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