AA USA Trading recalls dried kiwi slices due to undeclared FD&C dyes and sulfites. Consumers should check product labels for the specific recall codes.
AA USA Trading Inc. is recalling Dried Tai Sweet Mango Slice (FL 378858) because the product contains undeclared FD&C Yellow #6 and Dried Kiwi Slice (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 is recalling dried kiwi slices and dried tai sweet mango slices because they contain undeclared food dyes and sulfites. This poses a risk to consumers who may have allergic reactions or health issues from these additives.
The product contains undeclared FD&C dyes (blue #1 and yellow #5 in kiwi slices) and sulfites. These additives can cause allergic reactions in sensitive individuals, though the risk is not severe for most people.
Anyone who purchased these dried fruit slices between July 1 and December 11, 2014, from stores selling the product. People with allergies to the listed dyes or sulfites are at higher risk.
Check for the product name and net weight of 8 oz. on the label. The recall codes are FL 378858 for kiwi slices and FL 378859 for mango slices. The product was sold between July 1 and December 11, 2014.
Look for the recall codes FL 378858 (kiwi slices) or FL 378859 (mango slices) on the product label.
The product contains undeclared FD&C dyes and sulfites, which can cause allergic reactions in sensitive individuals.
Check the product label for the recall codes FL 378858 or FL 378859. If you have the product, you may want to contact the manufacturer for more information.
Yes, the additives can cause allergic reactions in people with sensitivities to the dyes or sulfites.
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-0528-2016 — AA USA Trading AA USA Trading Hello, I own a AA USA Trading that is covered by recall F-0528-2016 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.
