Pico De Gallo
Reason Potential contamination with Salmonella.
Roseli Sundried Tomato Pesto sauce recall
Recalled by Golden Plains Frozen Foods · Leeds, ND, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Golden Plains Frozen Foods is recalling Roseli Sundried Tomato Pesto sauce due that the product is positive for Salmonella. No illnesses, injury or complaints reported due that the product was contained and it did not distributed to the consumer.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
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
Roseli Sundried Tomato Pesto sauce. #408744 (Dot Item) , # 627328 (Roseli item),3- 2 lbs tubs (poly) packed in corrugated shipper. Keep Frozen - Thaw under refrigeration.
Quantity: 51 cases
Food: Sauces, dips & dressings
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.
5-19-2015
Where it was sold
Illinois
FDA's distribution note: Illinois
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
- Golden Plains Frozen Foods
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 1, 2015
- In FDA report of
- Jul 29, 2015
- Terminated
- Oct 13, 2015
- FDA recall number
- F-2859-2015 · event 71523
- Official record
- FDA enforcement report search
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