Baraka Mild Curry Powder packed in
Reason UBC FOOD Distributors initiated a voluntary recall of Baraka Hot and Mild Curry Powder packed in 7 oz. plastic tubs due to high levels of lead found in the products.
Baraka Hot Curry Powder packed in recall
Recalled by U.B.C. Food Distributors INC. · Dearborn, MI, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
UBC FOOD Distributors initiated a voluntary recall of Baraka Hot and Mild Curry Powder packed in 7 oz. plastic tubs due to high levels of lead found in the products.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
Baraka Hot Curry Powder packed in 7 OZ Plastic Jar
Quantity: 8 cases
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Baraka Hot Curry Powder packed in 7 oz. Plastic Jar, Upc 8 22514 26556 6 / case UPC 8 22514 266808 Product ID SPI .26556 (Hot)
Where it was sold
Colorado Illinois Indiana Michigan Minnesota Missouri Nebraska New York Ohio Virginia
FDA's distribution note: Domestic: CO, IL, IN, MI, MO, MN, NE, NY, OH Foreign/ VA/DOD: None
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- U.B.C. Food Distributors INC.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 19, 2018
- In FDA report of
- Dec 19, 2018
- Terminated
- Jun 2, 2020
- FDA recall number
- F-0715-2019 · event 81385
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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