Dried Kiwi Slice, Net Wt: 8 oz., AA USA Trading Inc. 47 Reid St. South River, NJ 08882 UPC 6 944155 210041
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0528-2016.
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.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0528-2016.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Aa Usa Trading Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0528-2016.
AA USA Trading Inc.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Aa Usa Trading Inc. Recall FAQ
Aa Usa Trading Inc. is the subject of a food safety report: Dried Kiwi Slice, Net Wt: 8 oz., AA USA Trading Inc. 47 Reid St. South River, NJ 08882 UPC 6 944155 210041. The notice was published on December 14, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 200 units are potentially affected.