FDA recall record

Lil Turtles Grandma Belle's Tomato Basil Soup, Net Wt recall — FDA H-0326-2026

Undeclared allergen - milk

Class IIclassification
H-0326-2026official record ID
Dec 31, 2025report date

Recall record at a glance

Official recordH-0326-2026
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLil Turtles LLC
Report dateDec 31, 2025
Recall initiation dateDec 4, 2025
Quantity110 cases
LocationBaltic, OH, United States

Official product description

Grandma Belle's Tomato Basil Soup, Net Wt. 17 oz. (482g), packaged in a glass jar, UPC 810084612293, Made By: Lil' Turtles 504 North Ray Street, Baltic, Ohio 43804, packed 12 jars per case

Why the product was recalled

Undeclared allergen - milk

Distribution information

IA, IL, IN, KS, KY, MN, MO, MS, NY, OH, OK, PA, UT, WI

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.