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Class IITerminated in FDA datasetRecall initiated Mar 22, 2015

Amy's Vegetable Lasagna, Light in Sodium, 9.5 oz (269 g) 12 boxes per case.

Recalling firm: Amys Kitchen Inc

Why it was recalled

Notified by supplier of spinach that product showing the presence of Listeria Monocytogenes was erroneously shipped and used in further manufacturing of products.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 5, 2015.

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Compare the exact product and package details with the label you have.

ProductAmy's Vegetable Lasagna, Light in Sodium, 9.5 oz (269 g) 12 boxes per case. UPC: 0-42272-00240-5, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA
Package size9.5 oz
UPC042272002405, 042272908073

FDA code information

Item number 000240; US distribution Lot code: 30-C145 Item number 00807F- Canadian distribution; Lot code 30-B-025.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Amy's Vegetable Lasagna, Light in Sodium, 9.5 oz (269 g) 12 boxes per case. UPC: 0-42272-00240-5, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA

Extracted codes and context

TypeCode / valueContext
UPC042272002405y's Vegetable Lasagna, Light in Sodium, 9.5 oz (269 g) 12 boxes per case. UPC: 0-42272-00240-5, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA
UPC042272908073 (269 g) 12 boxes per case. UPC: 0-42272-00240-5, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA
lot30-C145Item number 000240; US distribution Lot code: 30-C145 Item number 00807F- Canadian distribution; Lot code 30-B-025.

Original FDA recall reason

Notified by supplier of spinach that product showing the presence of Listeria Monocytogenes was erroneously shipped and used in further manufacturing of products.

Recall details

Recall number
F-2360-2015
Event ID
70806
FDA status
Terminated
Initiated
Mar 22, 2015
Reported
Jun 10, 2015
Classified
Jun 2, 2015
Terminated
Aug 5, 2015
Quantity
77 cases (12 boxes per case)
Location
Petaluma, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Nationwide and to Canada, Japan, Philippines and United Kingdom.

FDA source record · F-2360-2015

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

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