Meijer Ultra Trail Mix 18oz Pouch Recall: Coconut Not Listed in FALCPA
Meijer recalls 18oz Ultra Trail Mix pouches due to coconut not being listed in FALCPA. Check labels for the specific UPC and expiration date to determine if your product is affected.
Lower-risk recall
Coconut not listed in FALCPA Contains statement while a Contains statement is present on the label
Contact the company
What happened, in plain English
Meijer is recalling 18-ounce Ultra Trail Mix plastic pouches because the coconut content isn't listed in the FALCPA (Food Allergen Labeling and Consumer Protection Act). This could cause allergic reactions for people with coconut allergies. Read more at govinfonow.com/recall/20845-meijer-ultra-trail-mix-18oz-pouch-recall-coconut-not-listed.
Source Summary by GovInfoNow · govinfonow.com/recall/20845-meijer-ultra-trail-mix-18oz-pouch-recall-coconut-not-listed · Updated October 8, 2026 · FDA enforcement record: FDA #F-2454-2017
Cite this page
“Meijer Ultra Trail Mix 18oz Pouch Recall: Coconut Not Listed in FALCPA.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/20845-meijer-ultra-trail-mix-18oz-pouch-recall-coconut-not-listed. Based on FDA recall #F-2454-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2454-2017%22&limit=1).
Why it’s dangerous
The product contains coconut but the label does not list it under the FALCPA requirements. This means people with coconut allergies might consume it without knowing, leading to allergic reactions.
Who’s affected
People who own or use Meijer Ultra Trail Mix 18oz pouches with the specific UPC 7-08820-11510-1 and expiration date 10/17/2017 are affected. Those with coconut allergies are at higher risk.
How to tell if you have this one
Check for the product name 'MEIJER ULTRA TRAIL MIX 18 OZ plastic pouch' with UPC 7-08820-11510-1 and expiration date 10/17/2017 on the label.
- Brand
Meijer- Product
MEIJER ULTRA TRAIL MIX 18 OZ plastic pouch- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
IL, IN, KY, MI, OH, WI
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-2454-2017 | MEIJER ULTRA TRAIL MIX 18 OZ plastic pouch; UPC 7-08820-11510-1 Lot - Exp Date 09 7110 - 10/17/2017 | 4,468.50 lbs. |
| F-2455-2017 | MEIJER CASHEWS TOASTED COCONUT 8.25 OZ plastic pouch; UPC 7-19283-23754-5 Lot Code Exp Date 09 7145 - 10/31/2017 09 7102 - 10/31/2017 09 7080 - 10/31/2017 09 7009 - 9/22/2017 | 8,846.68 lbs. |
What to do — step by step
Check Label
Look for the UPC code 7-08820-11510-1 and expiration date 10/17/2017 on the product label.
Where it went and when
Where it was distributed
Distributed in 6 states.
FDA distribution: “IL, IN, KY, MI, OH, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, Indiana, Kentucky, Michigan, Ohio, Wisconsin.
Recall timeline
FDA terminated this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- 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-2454-2017 (June 13, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2454-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.