Odwalla Superfood Smoothie Recall: Tiny Metal Fragments Risk
Odwalla Superfood fruit smoothie bottles in Canada may contain tiny metal fragments. Recalled units have UPC 000-14054-06405-5. Consumers should check their bottles and contact Odwalla for details.
Lower-risk 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.
Contact the company
What happened, in plain English
The Coca-Cola Company is recalling Odwalla Superfood fruit smoothie bottles in Canada that may contain tiny metal fragments. This could pose a risk of injury if consumed. Affected bottles have a specific UPC code and were sold in 8-packs. Read more at govinfonow.com/recall/18980-odwalla-superfood-smoothie-recall-tiny-metal-fragments-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/18980-odwalla-superfood-smoothie-recall-tiny-metal-fragments-risk · Updated October 6, 2026 · FDA enforcement record: FDA #F-1656-2018
Cite this page
“Odwalla Superfood Smoothie Recall: Tiny Metal Fragments Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18980-odwalla-superfood-smoothie-recall-tiny-metal-fragments-risk. Based on FDA recall #F-1656-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1656-2018%22&limit=1).
Why it’s dangerous
Tiny metal fragments could be present in the smoothie bottles, which might cause injury if ingested. The hazard is limited to a small number of bottles and does not pose a significant risk under normal use conditions.
Who’s affected
Consumers in Canada who purchased Odwalla Superfood fruit smoothie bottles with the UPC 000-14054-06405-5 in 8-packs. Children and those with metal allergies are at slightly higher risk.
How to tell if you have this one
Check for the UPC code 000-14054-06405-5 on the bottle label. The product is sold in 8-packs of 15.2 oz. (450mL) plastic bottles. This recall applies only to Canadian distribution.
- Brand
Odwalla- Product
Odwalla Superfood fruit smoothie 15.2 oz. (450mL) plastic bottle; Sold in 8 pack case Unit UPC: 000-14054-06405-5- Category
Food
What to do — step by step
Check Bottle Label
Look for the UPC code 000-14054-06405-5 on the bottle label to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed in 33 states, and outside the U.S.
FDA distribution: “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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Alaska, Arizona, California, Colorado, Florida, Georgia, Hawaii, Illinois, Iowa, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nevada, New Mexico, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Texas, Utah, Virginia, Washington, Wisconsin, Wyoming.
Recall timeline
FDA terminated this recall 41 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1656-2018 (July 13, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1656-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.