Lower riskFood recall · FDA · Published October 21, 2024
Atwater's Spider Web Tarts Recall: Undeclared Almonds in Tarts
Atwater's Spider Web Tarts (26 tarts in clear plastic clamshell) recalled due to undeclared tree nuts (almonds). Consumers should check packaging for recall details.
“Atwater's Spider Web Tarts Recall: Undeclared Almonds in Tarts.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/8668-atwater-s-spider-web-tarts-recall-undeclared-almonds-in-tarts. Based on FDA recall #F-0216-2025 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0216-2025%22&limit=1).
The FDA announced on Oct. 21, 2024, that One Roof LLC is recalling Atwater's Spider Web Tarts due to undeclared almonds. The Class I recall affects products distributed in Maryland, Virginia, and Washington, D.C.
How to tell if you have it
Brand: Atwater's
Product: Spider Web Tarts
Quantity: 26 tarts packaged individually
Dimensions: 5.73 in x 5.95 in x 3 in clear plastic clamshell container
Julienne date: 292
Distribution states: MD, VA, DC
The hazard
The product contains undeclared tree nuts (almonds), posing an allergy risk to consumers. The FDA classified this as a Class I recall.
Context
GovInfoNow's records show One Roof LLC has one other recall on record since Dec. 21, 2025. On Dec. 21, 2025, the company issued an Atwater's Holiday Cookie Tin Recall for undeclared tree nut allergens including almonds, pecans, and walnuts. Other recent recalls of similar products include Albertsons Kitchen Salad Turkey Poppyseed Recall (May 6, 2026), Albertsons Cake Almond Raspberry Pavillions Recall (May 6, 2026), and L-Nutra Prolon Almond Cocoa Spread Recall (Aug. 7, 2026).
How to tell if you have this one
Check for the clear plastic clamshell container with 26 individual tarts. The product was sold with specific dates (Julienne date 292).
Brand
Atwater's
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Packaging
Look for the clear plastic clamshell container with 26 individual tarts.
Where it went and when
Where it was distributed
Distributed in D.C., Maryland and Virginia.
Listed by the agency
Not listed
FDA distribution: “The recalled product was distributed to the following states: MD, VA, DC,” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: District of Columbia, Maryland, Virginia.
Recall timeline
FDA terminated this recall 4 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-0216-2025 (October 21, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0216-2025 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.