AA USA Trading Inc. recalls Dried Tai Sweet Mango Slice (8 oz) due to undeclared FD&C dyes and sulfites. Consumers should check product labels for these ingredients.
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.
AA USA Trading Inc. is recalling Dried Tai Sweet Mango Slice (8 oz) because it contains undeclared food dyes and sulfites. This poses a risk of allergic reactions for people sensitive to these ingredients.
The product contains undeclared FD&C Yellow #6 and Dried Kiwi Slice contains undeclared FD&C Blue #1 and FD&C Yellow #5. It also contains undeclared sulfites. These ingredients can cause allergic reactions in sensitive individuals.
People who purchased Dried Tai Sweet Mango Slice (8 oz) between July 1 and December 11, 2014, from stores selling this product. Those with allergies to FD&C dyes or sulfites are most at risk.
Check for the product name 'Dried Tai Sweet Mango Slice' with a net weight of 8 oz. The UPC code is 6 944155 210102. Distribution dates were from July 1 to December 11, 2014.
Look for the product name 'Dried Tai Sweet Mango Slice' with a net weight of 8 oz and UPC code 6 944155 210102.
The product contains undeclared dyes and sulfites that may cause allergic reactions in sensitive individuals, so it is not safe for everyone.
The official recall does not specify a remedy, so check with the manufacturer or retailer for guidance.
The product was distributed from July 1 to December 11, 2014.
We’ve drafted a message you can send AA USA Trading to request your refund or repair — edit it as you like.
Subject: Recall F-0527-2016 — AA USA Trading AA USA Trading Hello, I own a AA USA Trading that is covered by recall F-0527-2016 from AA USA Trading. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
