Lower riskFood recall · FDA · Published January 9, 2024
Wegmans Outrageous Oat Cookies Recall: Undeclared Wheat Hazard
Wegmans recalls Outrageous Oat Cookies packaged in 5pk and bulk due to undeclared wheat. Consumers should avoid these products to prevent potential allergic reactions.
“Wegmans Outrageous Oat Cookies Recall: Undeclared Wheat Hazard.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/9793-wegmans-outrageous-oat-cookies-recall-undeclared-wheat-hazard. Based on FDA recall #F-0777-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0777-2024%22&limit=1).
Wegmans Food Markets, Inc. recalled Outrageous Oat Cookies due to undeclared wheat, the FDA said on Jan. 9, 2024. Consumers should stop eating the product and contact Wegmans for a refund.
How to tell if you have it
Outrageous Oat Cookies packaged in 5pk (UPC: 0-77890-56618-3)
Outrageous Oat Cookie only (UPC: 2-08165-00000-6, 2-08256-00000-7)
The hazard
The product contains undeclared wheat, which poses a risk to individuals with wheat allergies. The FDA classified this as a Class I recall, the most serious type.
Context
GovInfoNow's records show Wegmans Food Markets, Inc. has had 37 other recalls since April 21, 2014. Recent similar recalls include the Locatelli Grated Pecorino Romano recall (Nov. 22, 2025) and the Cheesecake Recall (Sept. 26, 2025). Other recent recalls of similar products include the Troemner Farm Pfeffernusse Cookies Recall (Dec. 19, 2025), the Lunds & Byerlys Monster Cookies Recall (Dec. 3, 2025), and the Bharat Bazar SOMA Kitchen Asafoetida Recall (Dec. 5, 2025).
How to tell if you have this one
Look for Outrageous Oat Cookies in 5-packs or bulk packaging with UPCs 0-77890-56618-3 or 2-08165-00000-6, 2-08256-00000-7. These products were sold by Wegmans Food Markets.
Brand
Wegmans
Product
Outrageous Oat Cookies packaged in 5pk and also sold in Bulk
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Labels
Look for the UPC numbers 0-77890-56618-3 or 2-08165-00000-6, 2-08256-00000-7 on the packaging.
Where it went and when
Where it was distributed
Distributed in 8 states and D.C..
Listed by the agency
Not listed
FDA distribution: “NY, PA, NJ, MD, MA, VA, NC, DE and DC” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Delaware, District of Columbia, Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, Virginia.
Recall timeline
FDA terminated this recall 3 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-0777-2024 (January 9, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0777-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.