Frozen Southern Style Biscuits
Reason Tennessee Dept. of Agriculture tested the product which was found positive for Listeria monocytogenes.
Frozen Buttermilk Biscuits recall
Recalled by Ingles Markets · Black Mountain, NC, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Tennessee Dept. of Agriculture tested the product which was found positive 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
Frozen Buttermilk Biscuits 25 oz. bag (12 count) and 44 oz. bag (20 count)
Quantity: 161 cases distributed (25 oz bags), 168 Cases distributed (44 oz. bags)
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.
UPC 8685404014 (25 oz.)and UPC 8685404894 (44 oz.; 20 ct.); All Best By Dates under these SKUs are being recalled.
Where it was sold
Georgia North Carolina South Carolina Tennessee
FDA's distribution note: GA, NC, SC, and TN
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
- Ingles Markets
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 18, 2017
- In FDA report of
- Jan 17, 2018
- Terminated
- Feb 9, 2018
- FDA recall number
- F-0561-2018 · event 78816
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.