BH Bold Chef Salad Kit
Reason Potential contamination with Salmonella.
Fresh Express Italian recall
Recalled by Chiquita Brands International, Inc. · Charlotte, NC, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product was found to be contaminated with 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
Fresh Express, Italian, Crunchy Romaine Lettuce and Red Cabbage Salad, 10oz clear plastic bags, UPC: 71279-21100.
Quantity: 60 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.
Product Code: H071A11A, Best buy date: 26-Mar
Where it was sold
Connecticut District of Columbia Delaware Massachusetts Maryland Maine North Carolina New Hampshire New Jersey New York Ohio Pennsylvania Rhode Island Virginia Vermont West Virginia
FDA's distribution note: CT, DE, MA, MD, ME, NC, NH, NY, NJ, OH, PA, RI, VA, VT WV and DC.
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
- Chiquita Brands International, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 28, 2014
- In FDA report of
- May 21, 2014
- Terminated
- May 29, 2014
- FDA recall number
- F-1932-2014 · event 67877
- Official record
- FDA enforcement report search
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