Severity
Critical
FDA Food recall · Reported July 17, 2013
Contamination with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened …
Lipari Foods, Inc. recalled Item Number: 368729 Item Description: TUB MD HAZELNUT/FILBERT RAW Case Pack: 12 Packag… - a critical-severity action.
Item Number: 368729 Item Description: TUB MD HAZELNUT/FILBERT RAW Case Pack: 12 Packag… was recalled by Lipari Foods, Inc. in July 17, 2013. Reason: Contamination with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections…. Check the official notice for the remedy. Verify recall #F-1697-2013 with the FDA Food before acting.
The recall
Lipari Foods, Inc. issued this critical-severity FDA Food recall-Contamination with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections….
Sourced from official FDA Food enforcement records. Verify recall #F-1697-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1697-2013) was formally reported on July 17, 2013, with the manufacturer initiating the action on June 4, 2013. It is classified under Critical severity (Class I), with a current status of Terminated. Lipari Foods, Inc. is listed as the recalling firm, operating out of Warren, MI. Federal records list the affected scope as 86 cases.
The documented reason for this recall is: Contamination with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individ… Distribution data in the federal record shows the product reached: Ohio, Michigan, West Virginia, Kentucky, Tennessee, Pennsylvania, Wisconsin, Illinois, and Indiana.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Critical
Affected scope
86 cases
Related Recalls
6
2 from same agency
Item Number: 368729 Item Description: TUB MD HAZELNUT/FILBERT RAW Case Pack: 12 Package Size: 9 OZ 2-Piece Clear Plastic Tub (No Label on Top, Nutritional Label on Bottom) UPC Number: 094776110049
Contamination with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirt
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1697-2013 |
| Date reported | July 17, 2013 |
| Date initiated | June 4, 2013 |
| Recalling firm | Lipari Foods, Inc. |
| Firm location | Warren, MI |
| Affected scope | 86 cases |
| Distribution | Ohio, Michigan, West Virginia, Kentucky, Tennessee, Pennsylvania, Wisconsin, Illinois, and Indiana. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported July 17, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.