Martina brand Fresh Whole Mangoes
Reason Product may be contaminated with Salmonella
Caribena Brand papayas packed in recall
Recalled by Caribe Produce · San Juan, TX, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product 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
Caribena Brand papayas packed in 35 lb. cartons marked with the brand "Caribena" and "Product of Mexico" stamped on the side. Each papaya bears a label which states "3112 CARIBENA Papaya MARADOL PRODUCT OF MEXICO www.grandeproduce.com" Papayas are packed in boxes of 8-12 papayas per box
Quantity: 1,152 cartons each with 35 lbs. of product
Food: Fresh fruit
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.
Each papaya bears a label which states "3112 CARIBENA Papaya MARADOL PRODUCT OF MEXICO www.grandeproduce.com". Lot # 115123
Where it was sold
North Carolina New Jersey
FDA's distribution note: NJ and NC
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
- Caribe Produce
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 15, 2012
- In FDA report of
- Jul 17, 2013
- Terminated
- Aug 15, 2013
- FDA recall number
- F-1643-2013 · event 61892
- Official record
- FDA enforcement report search
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