Recall record at a glance
| Official record | F-0587-2020 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Dierbergs Markets, Inc Corporate Office |
| Report date | Jan 22, 2020 |
| Recall initiation date | Dec 24, 2019 |
| Quantity | 456 salad kits |
| Location | Chesterfield, MO, United States |
Official product description
Dierbergs Kitchen Salad Togo Classic Ham & Turkey Chef Salad packaged in 9 oz containers UPC 2393393216 and 16 oz containers UPC 2393393217
Why the product was recalled
The firm received a recall notice for hardboiled eggs that were potentially contaminated with Listeria monocytogenes. The eggs were subsequently used to manufacture various salad and deli products.
Distribution information
Distributed to consumers at Dierbergs Market retail grocery stores.
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.