Food Recall Check
Class II · Moderate risk Terminated Initiated Oct 31, 2024 (2 years ago)

Curio Spice Co recall

Recalled by Curio Spice Co. · Winchester, MA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Product may be contaminated with mold.

Some molds produce toxins, and mold growth usually points to a problem with moisture, packaging or storage. All mold recalls.

What was recalled

Curio Spice Co. brand Grains of Paradise (Korerima) - Jar 1.25 oz net wt. UPC: 672975171032

Quantity: 760 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.

Batch number: PKRRM02202024 Better BY: 02/20/2027

Where it was sold

Alaska Alabama Arizona California Colorado Connecticut District of Columbia Delaware Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi Montana North Carolina Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Virginia Vermont Washington Wisconsin

FDA's distribution note: AL, AK, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
Curio Spice Co.
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 31, 2024
In FDA report of
Dec 4, 2024
Terminated
Mar 3, 2025
FDA recall number
F-0215-2025 · event 95662
Official record
FDA enforcement report search

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