Bel Brands USA Recall: Bel Brands USA is recalling Merkts Port Wine Cheese Spread after being notified by customers that white plastic pieces were found in the product. - F-0029-2018
United States
TerminatedClass II
- Company
- Bel Brands USA
- Product
- Merkts Port Wine Cheese Spread, Net Wt. 14 oz (396g), UPC 7…
- Recall date
- October 6, 2017
- Terminated
- November 16, 2017
- Source
- FDA
Reason for recall
Bel Brands USA is recalling Merkts Port Wine Cheese Spread after being notified by customers that white plastic pieces were found in the product.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Merkts Port Wine Cheese Spread, Net Wt. 14 oz (396g), UPC 76306-60200 | 76306-60200 | 1623 cases (12 cups per case) | Best Before: APR 29 18 LC2442A |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0029-2018
- Event ID
- 78246
- Status
- Terminated
- Classification
- Class II
- Company
- Bel Brands USA
- Product description
- Merkts Port Wine Cheese Spread, Net Wt. 14 oz (396g), UPC 76306-60200
- Quantity
- 1623 cases (12 cups per case)
- Reason
- Bel Brands USA is recalling Merkts Port Wine Cheese Spread after being notified by customers that white plastic pieces were found in the product.
- Recall initiation date
- October 6, 2017
- Report date
- October 25, 2017
- Classification date
- Not published in this source record
- Termination date
- November 16, 2017
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- UPC 76306-60200; Best Before: APR 29 18 LC2442A
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Bel Brands USA
Where this information comes from
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.
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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?
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
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How to interpret this historical record
This record is preserved as published by FDA, as of November 16, 2017.
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.
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