Food, drugs, devices › Dole Fresh Vegetables Inc
Food recall: Dole Chopped Kit Teriyaki Pineapple iceberg lettuce green leaf lettuce red cabbage sliced almonds teriyaki pineapple dre
Dole Fresh Vegetables Inc (Monterey, CA) initiated this food recall on 13 Apr 2023; FDA lists 1 product record under event 92123, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 53% of the 478 food enforcement events initiated in 2023 carry the same class.
Status: Terminated, terminated 24 Jul 2023. 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
"Undeclared allergen, milk, due to incorrect masterpack."
Distribution
"U.S. distribution to the following: FL, PA, VA, TN, LA No foreign distribution."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0842-2023 | Dole Chopped Kit Teriyaki Pineapple iceberg lettuce green leaf lettuce red cabbage sliced almonds teriyaki pineapple dressing crunchy noodles dried pineapples carrots Salad & Topping Net Wt.: 7.5 oz (212 g) Dressing Net: 1.9 fl oz (57 mL) Total Net Wt: 98.8 oz (276 g) Thoroughly Washed Perishable/Keep Refrigerated… | 181 cases | Class II | Terminated | 3 May 2023 |
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: "Undeclared allergen, milk, due to incorrect masterpack."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "U.S. distribution to the following: FL, PA, VA, TN, LA No foreign distribution."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 24 Jul 2023. "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.