CLASS II Food recall · Reported 1 Apr 2020 · FDA Enforcement Report

Cheddar Garlic Biscuits recalled by Southern Sisters Gourmet

Southern Sisters Gourmet is recalling Cheddar Garlic Biscuits, distributed in 9 states. The recall was initiated on 28 Jan 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesProducts are not coded.
Quantity recalledUnknown

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0913-2020
FDA event ID
84863
Recalling firm
Southern Sisters Gourmet, Coldwater, MS
Classification
Class II
Status
Terminated
Recall initiated
28 Jan 2020
FDA classified
17 Apr 2020
Reported
1 Apr 2020
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Product category
Cheese

Timeline

28 Jan 2020Recall initiated by company
1 Apr 2020Published in enforcement report+64 days
17 Apr 2020Classified by FDA+16 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

Southern Sisters Gourmet Cheddar Garlic Biscuits, Net Wt 16 oz (453.6 g)

Where it was distributed

Distributed in the states of AL, AR, FL, GA, IL, LA, MS, OK, and TX.

AlabamaArkansasFloridaGeorgiaIllinoisLouisianaMississippiOklahomaTexas

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Products are not coded.

Where was it sold?

Distributed in the states of AL, AR, FL, GA, IL, LA, MS, OK, and TX.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

7 other products · FDA event 84863

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