Martina brand Fresh Whole Mangoes
Reason Product may be contaminated with Salmonella
Organic Mango Freeze Dried Powder recall
Recalled by New Acai Amazonas LLC · Orlando, FL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential Salmonella contamination
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
Organic Mango Freeze Dried Powder, Bulk, 15-kilogram boxes (2 packs of 7.5 kilograms in a carton box), 7.5kg packaged in multi-wall kraft paper boxes with inner food-grade polyethylene liner, Store in a cool, dry place away from direct sunlight; keep sealed until use
Quantity: 255 kg (561 lb) (17 x 15 kg boxes)
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.
L10132851442505 (Supplier Lot M1013P030119525032283); Expiration Date(s): 13-07-2027
Where it was sold
Iowa
FDA's distribution note: Product distributed to IA
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
- New Acai Amazonas LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 15, 2025
- In FDA report of
- Sep 3, 2025
- Terminated
- Sep 12, 2025
- FDA recall number
- H-0538-2025 · event 97465
- Official record
- FDA enforcement report search
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