Recall record at a glance
| Official record | F-0648-2022 |
|---|---|
| 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
Ahold 5oz 50/50 Spinach & Spring Mix Product UPC 688267176524 Dole 5oz 50/50 Spinach & Spring Mix Blend Product UPC 071430010976 Lidl 11oz 50/50Baby Spinach/Spring Mix Blend Clamshell Product UPC 4056489503576 Dole 10oz 50/50 Spinach & Spring Mix Blend Clamshell Product UPC 071430010983 Marketside 11oz 50-50 Spinach & Spring Mix Blend Clamshell Product UPC 681131355018 Marketside 16oz Organic 50-50 Spinach & Spring Mix Clamshell Product UPC 681131354783 Marketside 5.5oz Organic 50-50 Spinach & Spring Mix Clamshell Product UPC 681131354790 Naturally Better 16oz Organic 50-50 Spinach & Spring Mix Clamshell Product UPC 607880203431 Naturally Better 5oz Organic 50-50 Spinach & Spring Mix Clamshell Product UPC 607880203363 Natures Promise 5oz Organic 50-50 Spinach & Spring Mix Clamshell Product UPC 688267154560
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.