United States
TerminatedClass III
5 lb. loaves of cheese may contain metal foreign material.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Pasteurized Process American Cheese, white, 2 - 5lb loaves per case. Brands as follows: 1) ingles; 2) Publix Deli; 3) Primo Taglio Classics; 4) Tropical | Not published in this source record | 2487 cases | Expiration Date: 1) 06/14/2020; 2) 06/14/2020, 06/20/2020; 3) 06/14/2020; 4) 06/14/2020 |
This recall shares FDA event ID 84046 with 5 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: September 25, 2020Historical recordClass III
FDA Recall United States TerminatedTerminated: September 25, 2020Historical recordClass III
FDA Recall United States TerminatedTerminated: September 25, 2020Historical recordClass III
FDA Recall United States TerminatedTerminated: September 25, 2020Historical recordClass III
FDA Recall United States TerminatedTerminated: September 25, 2020Historical recordClass III
Responsible company: Great Lakes Cheese Co Inc
FDA Recall United States TerminatedTerminated: April 24, 2026Historical recordClass II
FDA Recall United States TerminatedTerminated: April 24, 2026Historical recordClass II
FDA Recall United States TerminatedTerminated: April 24, 2026Historical recordClass II
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 |
|---|---|
| Massachusetts | 1 |
| Pennsylvania | 1 |
| Maryland | 1 |
| New York | 1 |
| Vermont | 1 |
| Maine | 1 |
| North Carolina | 1 |
| Georgia | 1 |
| Florida | 1 |
| Kentucky | 1 |
| New Jersey | 1 |
| Illinois | 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.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
FDA classifies this recall as Class III. See how to read an FDA recall record (linked above) for what each classification level means.
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.
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
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This record is preserved as published by FDA, as of September 25, 2020.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.
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