“Damascus Bakery Recalls Bantam Classic Bagels for Undeclared Egg Allergen.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/13246-damascus-bakery-recalls-bantam-classic-bagels-for-undeclared-egg-allergen. Based on FDA recall #F-0899-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0899-2022%22&limit=1).
The FDA announced on Feb. 25, 2022, that Damascus Bakery LLC voluntarily recalled Bantam Classic Bagels due to an undeclared egg allergen hazard. Owners should contact the company for a refund.
How to tell if you have it
Brand: Damascus Bakery
Product: Bantam Classic Bagels
Size: 6/1.3 oz pieces per carton (7.8 oz), Paper Carton
Product Code: Classic Bagels 213455
Lot Code: BB May/27/2023
Quantity: 232 cases
Distribution: SC, PA, MA, MN, NY, IN
The hazard
The bagels contain undeclared egg allergen, which poses a risk to individuals with egg allergies. The FDA classified this recall as Class II.
Context
GovInfoNow's records show Damascus Bakery LLC has one other recall on record since April 19, 2022, involving undeclared egg allergen in frozen bagels. Other recent recalls of similar products include B.C. Williams Bakery Bread Mix Recall (Dec. 23, 2025), Outside The Breadbox Bread Crumbs recall (Jan. 8, 2026), and WFM Purchasing Brussel Sprouts & Kale Slaw Recall (Dec. 31, 2025).
How to tell if you have this one
Check for the product code 213455 and lot code BB May/27/2023. The product comes in a paper carton containing six 1.3 oz pieces per carton (7.8 oz total).
Brand
Damascus Bakery
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop consuming the bagels
Do not eat the recalled Bantam Classic Bagels if you have an egg allergy or if your product matches the lot code.
Check your product details
Verify that your package has product code 213455 and lot code BB May/27/2023.
Where it went and when
Where it was distributed
Distributed in 6 states.
Listed by the agency
Not listed
FDA distribution: “The product was distributed to the following states: SC, PA, MA, MN, NY, IN.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Indiana, Massachusetts, Minnesota, New York, Pennsylvania, South Carolina.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
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-0899-2022 (February 25, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0899-2022 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 10, 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.