FDA Recall United States Terminated Historical recordClass I
SM Fish Corp.
- Product
- OSSIE'S EGG SALAD, NET WT. 7 OZ., UPC 73988570552; -- Far Ro…
- Published
- November 2, 2016
- Distribution
- New York and New Jersey via retail store…
SM Fish Corp. Recall: The product has the potential to be contaminated with Listeria monocytogenes based on the presence of the bacteria in the plant.
United States
TerminatedClass I
- Company
- SM Fish Corp.
- Product
- OSSIE'S PICKLED LOX DAIRY, NET WT. 8 OZ., UPC 739885114136;…
- Recall date
- July 29, 2016
- Terminated
- August 25, 2016
- Source
- FDA
Reason for recall
The product has the potential to be contaminated with Listeria monocytogenes based on the presence of the bacteria in the plant.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| OSSIE'S PICKLED LOX DAIRY, NET WT. 8 OZ., UPC 739885114136; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub. | 739885114136 | Not published in this source record | Not published in this source record |
Distribution
- New York and New Jersey
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1976-2016
- Status
- Terminated
- Classification
- Class I
- Company
- SM Fish Corp.
- Product description
- OSSIE'S PICKLED LOX DAIRY, NET WT. 8 OZ., UPC 739885114136; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
- Quantity
- Not published in this source record
- Reason
- The product has the potential to be contaminated with Listeria monocytogenes based on the presence of the bacteria in the plant.
- Recall initiation date
- July 29, 2016
- Report date
- August 31, 2016
- Classification date
- Not published in this source record
- Termination date
- August 25, 2016
- Distribution pattern
- New York and New Jersey
- UPC, lot, and code information
- UPC 739885114136
- Voluntary or mandated
- Not published in this source record
- Initial notification method
- Not published in this source record
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: SM Fish Corp.
Other recalls from SM Fish Corp.
FDA Recall United States Terminated Historical recordClass I
SM Fish Corp.
- Product
- OSSIE'S HOME MADE TUNA SALAD, NET WT. 7 OZ., UPC 73988570550…
- Published
- November 2, 2016
- Distribution
- New York and New Jersey via retail store…
FDA Recall United States Terminated Historical recordClass I
SM Fish Corp.
- Product
- OSSIE'S HONEY MUSTARD HERRING; NET WT. 7 OZ. 739885109019; -…
- Published
- November 2, 2016
- Distribution
- New York and New Jersey via retail store…
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.
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