Frozen Unbaked Biscuits sold under the brand names of Hilltop Hearth recall
Recalled by Holsum Baking Company Warehouse · Phoenix, AZ, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Firm was notified 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
Frozen Unbaked Biscuits sold under the brand names of Hilltop Hearth, Mary B's & Marshall.
Quantity: 456,580 cases of frozen biscuits
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.
Hilltop Hearth - Fill in; Mary B's Best By Dates 12/27/2017 09/17/2018; Marshall.- Fill in
Where it was sold
Alabama Arkansas Arizona California Colorado Connecticut Florida Georgia Iowa Illinois Indiana Kansas Michigan Minnesota Missouri Mississippi North Carolina North Dakota Nebraska New Jersey New Mexico Nevada Ohio Oklahoma Pennsylvania South Carolina Tennessee Texas Utah Virginia Wisconsin West Virginia
FDA's distribution note: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, MI, MN, MO, MS, NC, ND, NE, NJ, NM, NV, OH, OK, PA, SC, TN, TX, UT, VA, WI & WV.
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
- Holsum Baking Company Warehouse
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 3, 2018
- In FDA report of
- Feb 28, 2018
- Terminated
- Jul 3, 2018
- FDA recall number
- F-0823-2018 · event 78864
- Official record
- FDA enforcement report search