Recall record at a glance
| Official record | F-1544-2022 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | H-E-B Grocery Company, LP DBA HEB Milk & Culture Plant #80645 |
| Report date | Aug 24, 2022 |
| Recall initiation date | Aug 1, 2022 |
| Quantity | 880 retail cups |
| Location | San Antonio, TX, United States |
Official product description
HEB Creamy Creations Light 1/1 The Fat 1/3 Fewer Calories Of Regular Ice Cream Mint Chocolate Chip Ice Cream Half Gallon (1.89L) UPC 4122048399 packaged in a paper carton with a paper lid with a plastic edge
Why the product was recalled
Undeclared wheat
Distribution information
Texas and Mexico
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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.