FDA recall record

Sirob Imports Curry powder packaged under bulk, retail, and food service recall — FDA F-0696-2019

Products may contain elevated levels of lead.

Class Iclassification
F-0696-2019official record ID
Nov 21, 2018report date

Recall record at a glance

Official recordF-0696-2019
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmSirob Imports, Inc.
Report dateNov 21, 2018
Recall initiation dateOct 23, 2018
Quantity12,100 pounds (total for all products)
LocationLindenhurst, NY, United States

Official product description

Curry powder packaged under bulk, retail, and food service labels. Bulk: CURRY POWDER Net Weight 55 LBS, DISTRIBUTED BY SIROB IMPORTS LINDENHURST, NEW YORK USA (sold in a 55 pound bag) Packaged under the following retail brands: Corrado 16 oz. UPC: 0 12729 01100 7 8 oz. UPC: 0 12729 01102 1 Orlando Imports 16 oz. UPC: 0 53760 45255 8 Nouri s Syrian Bakery 8 oz. UPC: 0 12729 01102 1 16 oz. UPC: 0 1279 0110 7 Mediterranean Specialty Foods 8 oz. UPC: 0 12729 01102 1 Butera Fruit Market 8 oz. - UPC: 0 12729 45273 2 Packaged under the following food service brands: FC Finest Choice CURRY POWDER 16 oz. - UPC: 0 12729 01100 7 Packed By: SIROB IMPORTS, INC www.boborisfood.com CURRY POWDER 5 POUNDS - UPC: 0 12729 00996 7 Packed By: SIROB IMPORTS, INC www.boborisfood.com PREMIUM LABEL CURRY POWDER 16 oz. - PLCP12 Distributed by: Foodirect, Inc. Bronx, NY 10474 ROSE LEAF CURRY POWDER 16 OZ - UPC: 0 12729 01100 7 DIST BY: H. SCHRIER FOODS BROOKLYN, NY 11234 K FRESH CHOICE Finest Quality CURRY POWDER A Division Of AceEndico Corp. Elmsford, NY 17 OUNCES - UPC: 0 12729 00999 8 Manhattan Gourmet CURRY POWDER 16 Ounces - UPC: 0 12729 01100 7 Exclusively by VFS, Bronx, NY 10474 Valley Park CURRY POWDER 16 OZ - UPC: 0 12729 01100 7

Why the product was recalled

Products may contain elevated levels of lead.

Distribution information

NY, IL, NJ, MI,PA,FL

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.

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