Marketside Chopped Salad Kit Bacon Crunch
Reason Product has the potential to be contaminated with Listeria monocytogenes.
Dole American Blend recall
Recalled by Dole Fresh Vegetables Inc · Monterey, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Tennessee Department of Agriculture collected a random sample of Dole American Blen and had a positive result for Listeria Monocytogenes.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
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 American Blend; Iceberg, Romaine, Red Cabbage, Carrots and Radishes. Net Wt. 12 oz. (340g) UPC 0 71430 00933 8 Distributed by Dole Fresh Vegetables, Monterey, CA 93940
Quantity: 922 cases
Food: Leafy greens & salads
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.
Code: A275208A or B275208B; Enjoy by Date: 10-17-12.
Where it was sold
Illinois Indiana Maine Missouri New Jersey New York Ohio Pennsylvania Tennessee Wisconsin
FDA's distribution note: IL, IN, ME,. MO, NJ, NY, OH, PA, TN and WI
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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 Vegetables Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 17, 2012
- In FDA report of
- Nov 14, 2012
- Terminated
- Nov 19, 2012
- FDA recall number
- F-0615-2013 · event 63483
- Official record
- FDA enforcement report search
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Reason Product has the potential to be contaminated with Listeria monocytogenes.
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