Whole Foods Market Brand 365 Croissant 6-Pack Recalled for Undeclared Eggs
Whole Foods Market Brand 365 recalls 6-pack croissants due to undeclared eggs. Consumers should check UPC 0248421006991 and avoid use until notified.
Lower-risk recall
Product contains undeclared eggs.
Contact the company
What happened, in plain English
Whole Foods Market Brand 365 is recalling 6-pack croissant products because they contain undeclared eggs. This could affect people with egg allergies who might experience allergic reactions. Read more at govinfonow.com/recall/22949-whole-foods-market-brand-365-croissant-6-pack-recalled-for.
Source Summary by GovInfoNow · govinfonow.com/recall/22949-whole-foods-market-brand-365-croissant-6-pack-recalled-for · Updated October 9, 2026 · FDA enforcement record: FDA #F-0618-2017
Cite this page
“Whole Foods Market Brand 365 Croissant 6-Pack Recalled for Undeclared Eggs.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/22949-whole-foods-market-brand-365-croissant-6-pack-recalled-for. Based on FDA recall #F-0618-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0618-2017%22&limit=1).
Why it’s dangerous
The croissants contain eggs without being listed on the label. This poses a risk for individuals with egg allergies who could have an allergic reaction if they consume the product.
Who’s affected
People with egg allergies are most at risk from this recall. The affected product is sold in Whole Foods Market stores.
How to tell if you have this one
Check for UPC code 0248421006991 on the product packaging. The recall applies to 6-pack croissants sold by Whole Foods Market up to November 4, 2016.
- Brand
Whole Foods Market Brand 365- Category
Food
All 3 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.
- Status
Terminated- Distribution
Select Whole Foods Market stores in Pennsylvania, Maryland, Ohio, Kentucky, New Jersey, Virginia and Washington D.C.
| Recall number | Product, codes & lots | Quantity | Class |
|---|---|---|---|
| F-0618-2017 | CROISSANT 6 PK; UPC Code Product Desc Lot Code 0248421006991 CROISSANT 6 PK. sell by 11/4/16 and before | Total volume made and distributed from 8/1/2016-11/2/2016: Plain Croissant 6pk: 42118 units. | Class II |
| F-0619-2017 | MULTI GRAIN CROISSANT 6 PK; UPC Code Product Desc Lot Code 0241654006998 MULTIGRAIN CROISSANT 6PK sell by 11/4/16 and before | Total volume made and distributed from 8/1/2016-11/2/2016: Multigrain Croissant 6pk: 1547 units. | Class II |
| F-0620-2017 | CROISSANT CHOCOLATE 6 PK; UPC Code Product Desc Lot Code 0248422008994 CROISSANT CHOCOLATE 6 PK sell by 11/5 and before | Total volume made and distributed from 8/1/2016-11/2/2016: Chocolate Croissant 6pk: 7892 units. | Class I |
What to do — step by step
Check Product Label
Look for UPC code 0248421006991 on the croissant packaging.
Where it went and when
Where it was distributed
Distributed in 6 states and D.C..
FDA distribution: “Select Whole Foods Market stores in Pennsylvania, Maryland, Ohio, Kentucky, New Jersey, Virginia and Washington D.C.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: District of Columbia, Kentucky, Maryland, New Jersey, Ohio, Pennsylvania, Virginia.
Recall timeline
FDA terminated this recall 8 months 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.
Questions people ask
What should I do if I have the recalled product?
The recall does not require immediate action, but you should check the product label to confirm if it's affected.
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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-0618-2017 (November 2, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0618-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.