Food, drugs, devices › Dole Fresh Vegetables Inc
Food recall: Italian blend Salad (Romaine Lettuce and Radicchio) packaged under the following brand names: Dole Italian Blend, (UPC 7
FDA enforcement event 67748 is a food recall by Dole Fresh Vegetables Inc of Monterey, CA, initiated 13 Mar 2014 and classified Class I, with 1 product record.
FDA defines Class I as a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. 50% of the 573 food enforcement events initiated in 2014 carry the same class.
Status: Terminated, terminated 21 Apr 2014. Initiation: voluntary: firm initiated. Dole Fresh Vegetables Inc has 27 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Dole Fresh Vegetables Inc, Monterey, CA.
Reason for recall
"Canadian Food Inspection Agency tested a random sample of bagged Italian Blend which tested positive for Listeria Monocytogenes."
Distribution
"CT, FL, IL, IN, KY, MA, MD. MI, NC, NJ, NY, OH, PA, SC, VA and Canada"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1702-2014 | Italian blend Salad (Romaine Lettuce and Radicchio) packaged under the following brand names: Dole Italian Blend, (UPC 7143000819); Fresh Selections Italian Style Blend (Kroger) (UPC 1111091045); Little Salad Bar Italian Salad, (UPC 4149811014); Marketside Italian Style Salad, (Wal Mart) (UPC 8113102780) 10 oz. bags… | 3,807 cases (6 x 10 oz bag per case) | Class I | Terminated | 2 Apr 2014 |
Context
Other enforcement events for Dole Fresh Vegetables Inc
All 27 events for Dole Fresh Vegetables Inc
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Canadian Food Inspection Agency tested a random sample of bagged Italian Blend which tested positive for Listeria Monocytogenes."
What does Class I mean?
FDA classifies recalls by relative degree of health hazard. Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
Where was the product distributed?
FDA's distribution pattern field reads: "CT, FL, IL, IN, KY, MA, MD. MI, NC, NJ, NY, OH, PA, SC, VA and Canada"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 21 Apr 2014. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.