RecallRadar
FDA · FoodClass I

New Acai Amazonas LLC food recall: Organic Mango Freeze Dried Powder

SalmonellaMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
97465
Recall initiated
Aug 15, 2025
Classified by FDA
Aug 27, 2025
Posted in Enforcement Report
Sep 3, 2025
Terminated
Sep 12, 2025
Recalling firm
NEW ACAI AMAZONAS LLC
Firm location
Orlando, FL, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Potential Salmonella contamination

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Aug 15, 2025. FDA classified it 12 days later, on Aug 27, 2025. Distribution reported by FDA: Product distributed to IA

Recalled products (1)

  • H-0538-2025 Class I Terminated

    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

    Codes / lots: L10132851442505 (Supplier Lot M1013P030119525032283); Expiration Date(s): 13-07-2027

    Quantity: 255 kg (561 lb) (17 x 15 kg boxes)

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 97465
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.