Mild Jerk Curry Powder. Packaged under name Ocho Rios Mild Jerk Curry Seasoning. Sold as 2 oz, 4 oz, 6 oz, 8 oz, 22 oz, and 5 lb.
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (chemical exposure). 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-1617-2017.
Product samples tested positive for lead. Finished curry products tested and ground turmeric ingredient used to manufacture the curry seasoning also tested positive for lead.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1617-2017.
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 Oriental Packing Co., 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-1617-2017.
Oriental Packing Co., 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.
Oriental Packing Co., Inc. Recall FAQ
Oriental Packing Co., Inc. is the subject of a food safety report: Mild Jerk Curry Powder. Packaged under name Ocho Rios Mild Jerk Curry Seasoning. Sold as 2 oz, 4 oz, 6 oz, 8 oz, 22 oz, and 5 lb.. The notice was published on August 2, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 373,411 units are potentially affected.