Organic Triple Berry Blend Strawberries
Reason Potential E. coli O145:H28 Contamination
Dole Fresh Picked-Emballes frais Blueberries/Bleuets recall
Recalled by Dole Fresh Fruit Company · Crum Lynne, PA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Canadian Food Inspection Agency tested blueberries and found Cyclospora cayetanensis.
Pathogen: Cyclospora
A parasite linked to fresh produce.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Dole Fresh Picked-Emballes frais Blueberries/Bleuets: Packed in clear plastic container in the following sizes; 18 oz. - UPC: 0 71430 01154 6; Pint (16 oz.): UPC: 0 71430 01151 5; 6 oz. UPC: 07143001150 8; 24 oz. UPC: 071430011155 3 Distributed by Dole Berry Co, Winterhaven. FL Product of USA.
Quantity: Update 7-9-21 - correct number is 22,545
Food: Berries
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
18 oz. codes: 14632 14732 15032,15046 15232 15446,15432 15646,15648 Pint codes: 15032,15046 15132,15148,15146 15232 15332 15646,15648 6 oz. codes: 14632 15032,15046 15646,15648 24 oz. codes:15132,15148,15146 15332 15446,15432 15848, 15846
Where it was sold
Arkansas Illinois Wisconsin
FDA's distribution note: AR, WI, IL,. Canada to Vancouver, BC and Calgary, AB, Langley, BC, Acheson, AB,
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Dole Fresh Fruit Company
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 25, 2021
- In FDA report of
- Aug 4, 2021
- Terminated
- Dec 7, 2021
- FDA recall number
- F-0796-2021 · event 88183
- Official record
- FDA enforcement report search
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