AA USA Recalls Dried Mango for Undeclared Sulfites & Allergens
AA USA Trading recalls 200 bags of Dried Tai Sweet Mango Slice due to undeclared sulfites, FD&C Yellow #6, and other allergens.
Stop using this now
AA USA Trading Inc. is recalling Dried Tai Sweet Mango Slice (NYSDAM FL: 378858) because the product contains undeclared FD&C Yellow #6 and Dried Kiwi Slice (NYSDAM FL: 378859) because this product contains undeclared FD&C Blue #1, FD&C Yellow #5. Undeclared sulfites were also in the product.
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What happened, in plain English
AA USA Trading Inc. is recalling Dried Tai Sweet Mango Slice because it contains undeclared sulfites and food colorings (FD&C Yellow #6) that are not listed on the label. The company also recalled Dried Kiwi Slices for undeclared FD&C Blue #1 and Yellow #5. These undeclared ingredients pose a risk to consumers with specific allergies or sensitivities. Read more at govinfonow.com/recall/25586-aa-usa-recalls-dried-mango-for-undeclared-sulfites-allergens.
Source Summary by GovInfoNow · govinfonow.com/recall/25586-aa-usa-recalls-dried-mango-for-undeclared-sulfites-allergens · Updated October 11, 2026 · FDA enforcement record: FDA #F-0527-2016
Cite this page
“AA USA Recalls Dried Mango for Undeclared Sulfites & Allergens.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/25586-aa-usa-recalls-dried-mango-for-undeclared-sulfites-allergens. Based on FDA recall #F-0527-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0527-2016%22&limit=1).
Why it’s dangerous
Undeclared sulfites can cause severe allergic reactions in sensitive individuals, ranging from hives to anaphylaxis. Additionally, undeclared food colorings like FD&C Yellow #6, Blue #1, and Yellow #5 may trigger adverse reactions in people with specific dye sensitivities.
Who’s affected
Consumers who purchased the recalled dried fruit products, particularly those with sulfite allergies or sensitivities to FD&C Yellow #6, Blue #1, or Yellow #5. The recall affects items distributed in New Jersey and New York.
How to tell if you have this one
Check for Dried Tai Sweet Mango Slice, Net Wt: 8 oz., manufactured by AA USA Trading Inc. at 47 Reid St, South River, NJ 08882, with UPC 6 944155 210102. Also look for Dried Kiwi Slices (NYSDAM FL: 378859). The mango slices were distributed between July 1 and December 11, 2014.
- Brand
AA USA Trading- Product
Dried Tai Sweet Mango Slice, Net Wt: 8 oz., AA USA Trading Inc. 47 Reid St. South River, NJ 08882 UPC 6 944155 210102- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
NJ and NY
| Recall number | Product, codes & lots |
|---|---|
| F-0527-2016 | Dried Tai Sweet Mango Slice, Net Wt: 8 oz., AA USA Trading Inc. 47 Reid St. South River, NJ 08882 UPC 6 944155 210102; distribution dates 7/1-12/11/2014 |
| F-0528-2016 | Dried Kiwi Slice, Net Wt: 8 oz., AA USA Trading Inc. 47 Reid St. South River, NJ 08882 UPC 6 944155 210041; distribution dates 7/1-12/11/2014 |
What to do — step by step
Stop consuming the product
Do not eat the Dried Tai Sweet Mango Slice or Dried Kiwi Slices if you have them at home.
Check your ingredients
Verify if your package matches the UPC 6 944155 210102 or was part of the NYSDAM FL: 378858/378859 distribution.
Contact the manufacturer
Reach out to AA USA Trading Inc. for further instructions on disposal or return, as specific remedy details are not provided in this record.
Where it went and when
Where it was distributed
Distributed in New Jersey and New York.
FDA distribution: “NJ and NY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New Jersey, New York.
Recall timeline
FDA terminated this recall 18 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0527-2016 (December 14, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0527-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.