Food, drugs, devices › Dole Fresh Vegetables Inc
Food recall: Dole" Organic Romaine Hearts 3pk Organic Biologique) (UPC 0-71430-90061-1), Wild Harvest Organic Romaine Hearts, Net Wt
Dole Fresh Vegetables Inc (Monterey, CA) initiated this food recall on 21 Nov 2020; FDA lists 1 product record under event 86818, classified Class I.
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. 35% of the 381 food enforcement events initiated in 2020 carry the same class.
Status: Terminated, terminated 4 Feb 2021. 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
"Pathogenic non-O157 E.coli STEC found during routine sampling by Michigan Department of Agriculture and Rural Development."
Distribution
"U.S. distribution to the following: AZ, HI, IA, IL, IN, KS, MI, MN, MO, MS, MT, NC, ND, and VA No foreign distribution."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0144-2021 | Dole" Organic Romaine Hearts 3pk Organic Biologique) (UPC 0-71430-90061-1), Wild Harvest Organic Romaine Hearts, Net Wt 12 oz. (UPC 7-11535-50201-2), | 2,203 cases | Class I | Terminated | 9 Dec 2020 |
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: "Pathogenic non-O157 E.coli STEC found during routine sampling by Michigan Department of Agriculture and Rural Development."
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: "U.S. distribution to the following: AZ, HI, IA, IL, IN, KS, MI, MN, MO, MS, MT, NC, ND, and VA No foreign distribution."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 4 Feb 2021. "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.