Farmo Foods, Inc. Recall: Belfiore Cheese was notified by their direct account that cheese received had noticeable metal fragments in the product.
United States
TerminatedClass II
- Company
- Farmo Foods, Inc.
- Product
- Fresh Mozzarella; No brand name. Shipped in 30 lb. plastic…
- Recall date
- January 19, 2017
- Terminated
- May 9, 2017
- Source
- FDA
Reason for recall
Belfiore Cheese was notified by their direct account that cheese received had noticeable metal fragments in the product.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Fresh Mozzarella; No brand name. Shipped in 30 lb. plastic bucket | Not published in this source record | 12,000 lbs. | 005,006,009,010,012,016, and 017 with expiration dates of 2/9/17, 12/10/17, 12/13/17, 2/14/17, 2/16/17, 2/20/17, and 2/21/17 respectively. |
Distribution
- One customer in Oregon
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2201-2017
- Event ID
- 76984
- Status
- Terminated
- Classification
- Class II
- Company
- Farmo Foods, Inc.
- Product description
- Fresh Mozzarella; No brand name. Shipped in 30 lb. plastic bucket
- Quantity
- 12,000 lbs.
- Reason
- Belfiore Cheese was notified by their direct account that cheese received had noticeable metal fragments in the product.
- Recall initiation date
- January 19, 2017
- Report date
- May 17, 2017
- Classification date
- Not published in this source record
- Termination date
- May 9, 2017
- Distribution pattern
- One customer in Oregon
- UPC, lot, and code information
- 005,006,009,010,012,016, and 017 with expiration dates of 2/9/17, 12/10/17, 12/13/17, 2/14/17, 2/16/17, 2/20/17, and 2/21/17 respectively.
- 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
Responsible company: Farmo Foods, Inc.
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 II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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.
