CLASS I Food recall · Reported 14 Aug 2024 · FDA Enforcement Report

St. Jerome recalled by Kenny's Farmhouse Cheese

Kenny's Farmhouse Cheese is recalling St. Jerome, distributed in 7 states. The recall was initiated on 17 Jul 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot/Batch No. 231129
Quantity recalled130.68 lbs

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-1639-2024
FDA event ID
95031
Recalling firm
Kenny's Farmhouse Cheese, Austin, KY
Classification
Class I
Status
Terminated
Recall initiated
17 Jul 2024
FDA classified
2 Aug 2024
Reported
14 Aug 2024
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Cheese

Timeline

17 Jul 2024Recall initiated by company
2 Aug 2024Classified by FDA+16 days
14 Aug 2024Published in enforcement report+12 days

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

Reason for recall

Potential contamination with Listeria monocytogenes

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Kenny's Farmhouse Cheese - St. Jerome packaged in plastic vacuum sealed bags in 7oz wedges and whole 15lb wheels

Where it was distributed

AL, GA, ID, IN, KY, NC, TN

AlabamaGeorgiaIdahoIndianaKentuckyNorth CarolinaTennessee

Questions about this recall

Why was it recalled?

Potential contamination with Listeria monocytogenes

Which lots are affected?

Lot/Batch No. 231129

Where was it sold?

AL, GA, ID, IN, KY, NC, TN

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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.

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