Recall record at a glance
| Official record | F-0838-2019 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Hy-Vee Stores Inc. |
| Report date | Feb 13, 2019 |
| Recall initiation date | Jan 4, 2019 |
| Quantity | 2,608 32 oz and other similar sizes; 4,367 8 oz and other similar sizes |
| Location | West des Moines, IA, United States |
Official product description
HyVee brand mint-flavored cheese cakes packaged in the following ways: 1) Mint Cheesecake, Net Wt. 7 OZ, HyVee West Des Moines, IA UPC 02 80224 XXXXX packaged in clear plastic containers; 2) Mint Cheesecake Family Size, Net Wt. 28 OZ, HyVee West Des Moines, IA 02 80223 XXXXX, packaged in clear plastic containers
Why the product was recalled
Product contained an ingredient that tested positive for Salmonella.
Distribution information
Distributed to consumers in Iowa, Illinois, Missouri, Kansas, Nebraska, South Dakota, Minnesota and Wisconsin.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Press Release.
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.