Recall record at a glance
| Official record | F-0659-2022 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Dole Fresh Vegetables Inc. |
| Report date | Feb 16, 2022 |
| Recall initiation date | Dec 22, 2021 |
| Quantity | Total: 207,624 cases from Yuma and 2,081,894 cases from Bessemer City |
| Location | Monterey, CA, United States |
Official product description
Dole 10oz Caesar Kit Product UPC 071430008065 Lidl 10oz Caesar Kit Product UPC 20737740 Little Salad Bar 10.65oz Caesar Kit Product UPC 4099100263923 Little Salad Bar 10oz Caesar Kit Product UPC 4099100087000 Dole 11.3oz Ultimate Caesar Kit Product UPC 071430017029 Marketside 15oz Caesar Kit Product UPC 681131387446 Marketside 23.5oz Family Caesar Kit Product UPC 681131387460
Why the product was recalled
Potential Listeria monocytogenes
Distribution information
AL, AZ, CA, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI.
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: 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.