Atwater's Spider Web Tarts, 26 tarts packaged individually, 5.73 in x 5.95 in x 3 in clear plastic clamshell container,
Summary
The FDA issued a Class I for Atwater's Spider Web Tarts, 26 tarts packaged individually, 5.73 in x 5.95 in x by One Roof LLC. Reason: Undeclared tree nuts (almonds).
Details
Source
Food Recall
External ID
F-0216-2025
Action Date
2024-12-04
Status
Terminated
Category
food
Product Description
Atwater's Spider Web Tarts, 26 tarts packaged individually, 5.73 in x 5.95 in x 3 in clear plastic clamshell container, Julienne date 292
Lot/Code Info: Julienne date 292
Quantity Affected: 26 tarts
Reason for Recall
Undeclared tree nuts (almonds)
Distribution
The recalled product was distributed to the following states: MD, VA, DC,
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-21
Company
Baltimore, MD
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 82 food recalls issued in the same week, part of 204 food-related FDA actions this month.
One Roof LLC has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (One Roof LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does One Roof LLC have FDA actions?
One Roof LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0216-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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