Bleating Heart Cheese LLC recalls mixed milk cheese products due to Listeria Monocytogenes contamination found in FDA samples. Consumers should avoid these products from February 14 to September 19, 2014.
FDA samples found the presence of Listeria Monocytogenes in three varieties of cheese.
Bleating Heart Cheese LLC is recalling mixed milk cheese products that were found to contain Listeria Monocytogenes by FDA samples. This bacteria can cause serious illness, so affected products should not be consumed.
Listeria Monocytogenes is a bacterium that can cause severe food poisoning, especially in pregnant women, newborns, and people with weakened immune systems. FDA samples detected this bacteria in three varieties of the cheese.
Consumers who purchased Bleating Heart Cheese products from February 14 to September 19, 2014. Those with weakened immune systems are at higher risk for serious illness.
Check for products with codes 14-0214 to 14-0919 produced between February 14 and September 19, 2014. The product names include 'Funky Bleats - Mixed milk cheese with funk.'
Discard all Bleating Heart Cheese products with codes 14-0214 to 14-0919 produced between February 14 and September 19, 2014.
No, FDA samples found Listeria Monocytogenes in these products, which can cause serious illness. Do not consume.
The affected products were produced between February 14, 2014 (coded 14-0214) and September 19, 2014 (coded 14-0919).
Check the product code on the label; affected products have codes 14-0214 to 14-0919 produced between February 14 and September 19, 2014.
We’ve drafted a message you can send Bleating Heart Cheese to request your refund or repair — edit it as you like.
Subject: Recall F-0952-2015 — Bleating Heart Cheese Bleating Heart Cheese Hello, I own a Bleating Heart Cheese that is covered by recall F-0952-2015 from Bleating Heart Cheese. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.