Class ITerminated in FDA datasetJun 4, 2013

Item Number: 357642 Item Description: TUB SM ALMOND WHOLE RAW Case Pack: 12 Package Size: 10 OZ 2-Piece Clear Plastic Tub (No Label on Top, Nutritional Label on Bottom)

Recalling firm: Lipari Foods, Inc.

Why it was recalled

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

Check the codes ↓

The exact product

Item Number: 357642 Item Description: TUB SM ALMOND WHOLE RAW Case Pack: 12 Package Size: 10 OZ 2-Piece Clear Plastic Tub (No Label on Top, Nutritional Label on Bottom) UPC Number: 760208107450

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Lot Numbers: 23201305, 24201305 Best By Dates: 05/23/2014, 05/24/2014

TypeCode / valueContext
UPC760208107450e Clear Plastic Tub (No Label on Top, Nutritional Label on Bottom) UPC Number: 760208107450
lot23201305Lot Numbers: 23201305, 24201305 Best By Dates: 05/23/2014, 05/24/2014
lot24201305Lot Numbers: 23201305, 24201305 Best By Dates: 05/23/2014, 05/24/2014

Recall details

Recall number
F-1688-2013
Event ID
65392
FDA status
Terminated
Initiated
Jun 4, 2013
Reported
Jul 17, 2013
Classified
Jul 11, 2013
Terminated
Oct 17, 2013
Quantity
186 cases
Location
Warren, MI, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Ohio, Michigan, West Virginia, Kentucky, Tennessee, Pennsylvania, Wisconsin, Illinois, and Indiana.

FDA source record · F-1688-2013

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.