Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 28, 2020 (7 years ago)

Southern Sisters Gourmet Shrimp and Stone-Ground Grits recall

Recalled by Southern Sisters Gourmet · Coldwater, MS, United States

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

Why it was recalled

Undeclared allergen: Milk. Undeclared colors: Yellow #5 and #6.

Undeclared allergen: Milk

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

Southern Sisters Gourmet Shrimp and Stone-Ground Grits, Seasoning - Net Wt: 12 g, Grits - Wt: 8 ounces

Quantity: Unknown

Food: Seafood & fish 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.

Products are not coded.

Where it was sold

Alabama Arkansas Florida Georgia Illinois Louisiana Mississippi Oklahoma Texas

FDA's distribution note: Distributed in the states of AL, AR, FL, GA, IL, LA, MS, OK, and TX.

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. The risk from an undeclared allergen is to people allergic to milk; 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
Southern Sisters Gourmet
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 28, 2020
In FDA report of
Apr 1, 2020
Terminated
Feb 16, 2021
FDA recall number
F-0915-2020 · event 84863
Official record
FDA enforcement report search

Also recalled with it (7 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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