Good Fields Farm Wild Meadow Raw Goat Milk Cheese Recall: Listeria Risk
Good Fields Farm recalls Wild Meadow Raw Goat Milk Cheese due to Listeria monocytogenes detected in a sample. Consumers should check for code 101 on packaging to identify affected products.
Use caution until it’s fixed
The firm recalled cheese after a sample tested positive for Listeria monocytogenes by the State of New York.
Contact the company
What happened, in plain English
Good Fields Farm is recalling Wild Meadow Raw Goat: Goat Milk Cheese because a sample tested positive for Listeria monocytogenes. This bacteria can cause serious illness, so affected products should be discarded to prevent potential food poisoning. Read more at govinfonow.com/recall/19605-good-fields-farm-wild-meadow-raw-goat-milk-cheese-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/19605-good-fields-farm-wild-meadow-raw-goat-milk-cheese-recall · Updated October 7, 2026 · FDA enforcement record: FDA #F-1005-2018
Cite this page
“Good Fields Farm Wild Meadow Raw Goat Milk Cheese Recall: Listeria Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19605-good-fields-farm-wild-meadow-raw-goat-milk-cheese-recall. Based on FDA recall #F-1005-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1005-2018%22&limit=1).
Why it’s dangerous
Listeria monocytogenes is a bacteria that can cause severe food poisoning, especially in pregnant women, newborns, and people with weakened immune systems. The sample tested positive in New York, indicating the risk exists in this product.
Who’s affected
Consumers who purchased Wild Meadow Raw Goat Milk Cheese with code 101 on the packaging are affected. Those with compromised immune systems are at higher risk for serious illness from Listeria.
How to tell if you have this one
Check for the code '101' on the packaging of Wild Meadow Raw Goat Milk Cheese. The product is sold in various sizes with sealed flexible plastic packaging.
- Brand
Good Fields Farm- Category
Food
What to do — step by step
Check Packaging Code
Look for the code '101' on the packaging to identify affected products.
Where it went and when
Where it was distributed
Distributed in New York.
FDA distribution: “NY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New York.
Recall timeline
FDA terminated this recall 7 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #F-1005-2018 (March 5, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1005-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.