FDA Recall United States Terminated Historical recordClass II
Farm Country Cheese House, Inc.
- Product
- Marble Cheese, thirty-three 40 lb. blocks
- Published
- November 23, 2016
- Distribution
- Domestic: MI
Farm Country Cheese House, Inc. Recall: Farm Country Cheese House is conducting a voluntary recall of multiple vats of cheese due to potential contamination with Listeria monocytogenes.
United States
TerminatedClass I
- Company
- Farm Country Cheese House, Inc.
- Product
- White Cheddar Cheese, 40 lb. blocks
- Recall date
- October 10, 2016
- Terminated
- May 2, 2017
- Source
- FDA
Reason for recall
Farm Country Cheese House is conducting a voluntary recall of multiple vats of cheese due to potential contamination with Listeria monocytogenes.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| White Cheddar Cheese, 40 lb. blocks | Not published in this source record | 1247.53 lbs. | Made on 09/23/2016, Vat A |
Distribution
- Domestic: MI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0428-2017
- Event ID
- 75427
- Status
- Terminated
- Classification
- Class I
- Company
- Farm Country Cheese House, Inc.
- Product description
- White Cheddar Cheese, 40 lb. blocks
- Quantity
- 1247.53 lbs.
- Reason
- Farm Country Cheese House is conducting a voluntary recall of multiple vats of cheese due to potential contamination with Listeria monocytogenes.
- Recall initiation date
- October 10, 2016
- Report date
- November 23, 2016
- Classification date
- Not published in this source record
- Termination date
- May 2, 2017
- Distribution pattern
- Domestic: MI
- UPC, lot, and code information
- Made on 09/23/2016, Vat A
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 75427 with 4 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
Farm Country Cheese House, Inc.
- Product
- Hot Pepper Cheese, forty-five 40 lb. blocks
- Published
- November 23, 2016
- Distribution
- Domestic: MI
FDA Recall United States Terminated Historical recordClass II
Farm Country Cheese House, Inc.
- Product
- White Cheddar, thirty-nine, 40 lb. blocks from Vat A and 25…
- Published
- November 23, 2016
- Distribution
- Domestic: MI
FDA Recall United States Terminated Historical recordClass II
Farm Country Cheese House, Inc.
- Product
- Monterey Jack Cheese, 40 lb. blocks
- Published
- November 23, 2016
- Distribution
- Domestic: MI
Responsible company: Farm Country Cheese House, Inc.
Other recalls from Farm Country Cheese House, Inc.
FDA Recall United States Terminated Historical recordClass II
Farm Country Cheese House, Inc.
- Product
- Marble Cheese, thirty-three 40 lb. blocks
- Published
- November 23, 2016
- Distribution
- Domestic: MI
FDA Recall United States Terminated Historical recordClass II
Farm Country Cheese House, Inc.
- Product
- Hot Pepper Cheese, forty-five 40 lb. blocks
- Published
- November 23, 2016
- Distribution
- Domestic: MI
FDA Recall United States Terminated Historical recordClass II
Farm Country Cheese House, Inc.
- Product
- White Cheddar, thirty-nine, 40 lb. blocks from Vat A and 25…
- Published
- November 23, 2016
- Distribution
- Domestic: MI
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Michigan | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
