Southern Style Frozen Biscuits sold under the following brand names recall
Recalled by Sister Schubert's Rolls Division of T.Marzetti Company · Saraland, AL, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Firm was notified by their supplier of a positive test result for Listeria monocytogenes.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Southern Style Frozen Biscuits sold under the following brand names: Food Club, Food Lion, Laura Lynn, Lowes Foods, Marshalls, Morning Fresh Farms, Piggly Wiggly, Premium Pick 5, SE Grocers, Shur Fine, Southern Home & Valu Time
Quantity: 101,126 cases
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.
All product shipped between 4/11/2017 - 12/21/2017
Where it was sold
Alabama California Florida Georgia Indiana Kentucky Louisiana North Carolina Pennsylvania South Carolina Tennessee Texas Virginia
FDA's distribution note: Product was shipped to the following states: AL, CA, FL, GA, IN, KY, LA, NC, PA, SC TN, TX & VA.
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
- Sister Schubert's Rolls Division of T.Marzetti Company
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 28, 2017
- In FDA report of
- Feb 14, 2018
- Terminated
- Jul 11, 2018
- FDA recall number
- F-0788-2018 · event 78836
- Official record
- FDA enforcement report search