FDA recall record

Dole 15oz Family Classic Romaine Product UPC 071430010372 Dole recall — FDA F-0682-2022

Potential Listeria monocytogenes

Class Iclassification
F-0682-2022official record ID
Feb 16, 2022report date

Recall record at a glance

Official recordF-0682-2022
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmDole Fresh Vegetables Inc.
Report dateFeb 16, 2022
Recall initiation dateDec 22, 2021
QuantityTotal: 207,624 cases from Yuma and 2,081,894 cases from Bessemer City
LocationMonterey, CA, United States

Official product description

Dole 15oz Family Classic Romaine Product UPC 071430010372 Dole 9.0oz Premium Romaine Product UPC 071430009109 Dole 9oz Classic Romaine Product UPC 071430010693 Dole 9oz Hearts of Romaine Product UPC 071430009567 Kroger 10oz Hearts of Romaine Product UPC 011110910448 Kroger 10oz Leafy Romaine Product UPC 011110910462 Marketside 18oz Premium Romaine Salad Product UPC 681131388078 Marketside 9oz Premium Romaine Salad Product UPC 681131387538

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.

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