Pico de Gallo salsa
Reason The firm recalled because products manufactured used the cilantro recalled by their supplier has the potential to be contaminated with Salmonella.
Cheese and red onion enchilada recall
Recalled by Real Mex Foods · Vernon, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The firm recalled because products manufactured used the cilantro recalled by their supplier has the potential to be contaminated with Salmonella.
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
Cheese and red onion enchilada, 2 oz packaged in 240/2oz case, net weight 30 lbs. Product labeling reads in part:" REAL MEX FOODS Item # 14800 CHEESE & RED ONION ENCHILADA***KEEP REFRIGERATED*** PACK SIZE: 240/2 OZ. NET WEIGHT:30.00 LBS Real Mex Foods 3305 E. Vernon Ave. Vernon, Ca 90058.***"
Quantity: 21 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.
Use by date 08/24/12, Item # 14800, UPC 7 58897 14800
Where it was sold
FDA's distribution note: Distribution to food service such as restaurants.
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
- Real Mex Foods
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 14, 2012
- In FDA report of
- Sep 5, 2012
- Terminated
- Aug 12, 2013
- FDA recall number
- F-2034-2012 · event 62883
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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