Simply Fresh Salads
Reason Internal product label review discovered that wheat is not declared as an ingredient or allergen in Cranberry Walnut salad. Flatbread chips which contain wheat are visible through clear plastic container.
Five Star Gourmet Foods Energizer Box Item Code recall
Recalled by Five Star Gourmet Foods, Inc. · Ontario, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential Listeria monocytogenes contamination.
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
Five Star Gourmet Foods Energizer Box Item Code: FG10144
Quantity: 9186 cases
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.
Lot Numbers: 11216 11116 11316 11716 11116 11316 11716 11916 12016 12016 12416 11916 12416 12616 12516 12616 12716 12416 12516
Where it was sold
California
FDA's distribution note: U.S. distribution to the following; CA. No foregin distribution.
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
- Five Star Gourmet Foods, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 2, 2016
- In FDA report of
- Dec 21, 2016
- Terminated
- Dec 21, 2016
- FDA recall number
- F-0684-2017 · event 74455
- Official record
- FDA enforcement report search