FDA recall record

Gel Spice Co Inc 48 Hook Road, Bayonne, NJ 07002 2) Spice Supreme Ground recall — FDA F-1612-2017

Ground Turmeric may contain excess levels of lead.

Class Iclassification
F-1612-2017official record ID
Mar 22, 2017report date

Recall record at a glance

Official recordF-1612-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmGel Spice Co, Inc.
Report dateMar 22, 2017
Recall initiation dateJul 28, 2016
Quantity34,712 pounds total for all recalled products
LocationBayonne, NJ, United States

Official product description

1) Ground Tumeric item #73535 Net Wt 50 lbs Distributed by Gel Spice Co., Inc 48 Hook Road, Bayonne, NJ 07002 2) Spice Supreme Ground Turmeric Net Wt 2 oz. (56 g) Packed in the USA by Gel Spice Co., Inc. Bayonne, NJ 07002 UPC 076114364628 3)Clear Value Ground Turmeric Net Wt. .75 oz (21 g) Distributed by TopCo Associates LLC Elk Grove Village, IL 60007, UPC 036800354920 4) Market Pantry Ground Turmeric, Net Wt. 0.95 oz. Distributed by Target Corporation Minneapolis, MN 55403 Product of India UPC 085239211038 5) Spice Select Ground Turmeric, Net Wt 8 oz.(227g), Distributed By: GelSpice, Co., Inc., Bayonne, NJ 07002, UPC 076114007730 6) Lieber's Turmeric, Net Wt. 2 oz (56g), Dist by Lieber's Chocolate & Food Products Co, Maspeth, New York 11378, UPC 04342700626 7) Gel brand Ground Turmeric, Net Wt. 15 oz., (425g) Plastic Bottle, Packed by Gel Spice Co., Inc., Bayonne, NJ 07002, UPC 076114800867 8) b'gan seasonings Ground Turmeric NET WT. 16 oz 1 LB (454 g) Dist. by S. Bertram. Inc, Linden, NJ 07036 UPC 9) Freshly Ground Turmeric Net Weight 2.8oz (79g) Orient Provision & Trading Co. LTD UPC 6281063884002 10) Spice Supreme Ground Turmeric Net Wt 2 oz. (56 g) Gel Spice Co., Inc. Bayonne, NJ 07002 UPC 07611436462 11) Fresh Finds Ground Turmeric Net Wt. 3.75 oz (106g) Distributed by: Big Lots Stores, Inc. PO Box 28523 Columbus OH 43228-0523 UPC 08102601230

Why the product was recalled

Ground Turmeric may contain excess levels of lead.

Distribution information

nationwide

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: Press Release.

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

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