Lower riskFood recall · FDA · Published March 31, 2015
Whole Food Market Muffin Bran Recall: Undeclared Milk and Eggs
Whole Food Market recalls 6-pack muffin bran with undeclared milk and eggs. Consumers should check product codes and contact Whole Foods Market for details.
“Whole Food Market Muffin Bran Recall: Undeclared Milk and Eggs.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/27173-whole-food-market-muffin-bran-recall-undeclared-milk-and-eggs. Based on FDA recall #F-2441-2015 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2441-2015%22&limit=1).
The Food and Drug Administration announced on March 31, 2015, that Whole Food Market voluntarily recalled BRAN Whole Foods Market Muffin Bran due to undeclared milk and eggs. The agency issued recall number F-2441-2015 for the Class I hazard.
How to tell if you have it
Brand: Whole Food Market
Product: BRAN Whole Foods Market Muffin Bran 6Pk
Packaging: Clear plastic "clam shell" containers, NET WT. 12 oz.
PLU: 24857800499
Best By dates: 01/21/15 to 4/6/15
Distribution: AR, LA, OK, TX
Units affected: 6317 packages
The hazard
According to the FDA, the recalled muffins contain undeclared milk and eggs. The agency classified this as a Class I recall, indicating a reasonable probability that the product could cause serious adverse health consequences or death.
Context
GovInfoNow's records show Whole Food Market has 15 other recalls on record since July 18, 2014. Other recent recalls of similar products include Outside The Breadbox Bread Crumbs recall (Jan. 8, 2026), Blue Oven Artisan Bakery English Muffins Recall (Oct. 30, 2025), and Loard's Lemon Chiffon Ice Cream Recall (April 15, 2026).
How to tell if you have this one
Check for the product code 24857800499 on the packaging. The product was sold between January 21, 2015 and April 6, 2015 at Whole Foods Market stores in Austin, Texas.
Brand
Whole Food Market
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Code
Look for the product code 24857800499 on the packaging to confirm if it's recalled.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “AR, LA, OK, TX” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arkansas, Louisiana, Oklahoma, Texas.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-2441-2015 (March 31, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2441-2015 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.