Recall record at a glance
| Official record | F-1616-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Oriental Packing Co., Inc. |
| Report date | Mar 22, 2017 |
| Recall initiation date | Aug 2, 2016 |
| Quantity | Approximately 373,411 lbs total |
| Location | Miami, FL, United States |
Official product description
Hot/Spicy Jerk Curry Powder. Packaged under the names: Blue Mountain Country Hot Jamaican Jerk Curry Seasoning & Ocho Rios Spicy Jerk Curry Seasoning. Sold as 2 oz, 4 oz, 6 oz, 8 oz, 22 oz, and 5 lb.
Why the product was recalled
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.
Distribution information
FL & NY.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.