Food Recall Check
Class I · High risk Terminated Initiated Jan 28, 2015 (12 years ago)

GROUND CUMIN Net Wt recall

Recalled by Sahadi Fine Foods, Inc. · Brooklyn, NY, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Cumin may contain undeclared peanut protein.

Undeclared allergen: Peanut

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

GROUND CUMIN, Net Wt. 5 lbs (2.3 Kg), UPC 7 52186 82560 0.

Quantity: 509 units

Food: Spices & seasonings

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.

Item 82560; Lot numbers: 420307, 425409, 430811, 421207, 427410, 431111, 422508, 427510, 433011, 423708, 428110, 433912, 425109, 428210, 435212

Where it was sold

Alabama Colorado Connecticut Florida Georgia Massachusetts Maine Missouri North Carolina New Jersey New York Ohio Pennsylvania Rhode Island South Carolina Texas Virginia

FDA's distribution note: AL, CO, CT, FL, GA, MA, ME, MO, NC, NJ, NY, OH, PA, RI, SC, TX, VA

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. The risk from an undeclared allergen is to people allergic to peanut; for anyone else the product is generally not a safety concern. 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
Sahadi Fine Foods, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 28, 2015
In FDA report of
Apr 22, 2015
Terminated
May 9, 2017
FDA recall number
F-1950-2015 · event 70407
Official record
FDA enforcement report search

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