Check the Batch
Class IITerminated in FDA datasetOct 25, 2013

ITALIA PASTA KIT, 310168 SAFEWAY 1/5.69#, NET WT: 5.69, S2560

Recalling firm: Taylor Farms Maryland-Assateague Drive

Why it was recalled

The firm manufactured and distributed 6 salad kits which contained salad dressing supplied by Reser's which was recalled due to possible Listeria Monocytogenes contamination.

Check your package

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

ProductITALIA PASTA KIT, 310168 SAFEWAY 1/5.69#, NET WT: 5.69, S2560, DISTRIBUTED BY LUCERNE FOODS, INC. PO BOX 99, PLEASANTON, CA945, 95466-009, 1-877-232-4271

FDA code information

TFMDAA288A, BEST IF USED BY: 10/25/2013; TFMDAA289A, BEST IF USED BY: 10/26/2013; TFMDAA290A, BEST IF USED BY: 10/27/2013; TFMDAA291A, BEST IF USED BY: 10/28/2013; TFMDAA295A, BEST IF USED BY: 11/01/2013; TFMDAA296A, BEST IF USED BY: 11/02/2013; TFMDAA297A, BEST IF USED BY: 11/03/2013

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

Full FDA record and distribution details

Original product description

ITALIA PASTA KIT, 310168 SAFEWAY 1/5.69#, NET WT: 5.69, S2560, DISTRIBUTED BY LUCERNE FOODS, INC. PO BOX 99, PLEASANTON, CA945, 95466-009, 1-877-232-4271

Extracted codes and context

TypeCode / valueContext
best by10/25/2013TFMDAA288A, BEST IF USED BY: 10/25/2013; TFMDAA289A, BEST IF USED BY: 10/26/2013; TFMDAA290A, BEST IF USED BY: 10/27/2013; TFMDAA291A, BEST IF USED BY: 10/28/2
best by10/26/2013TFMDAA288A, BEST IF USED BY: 10/25/2013; TFMDAA289A, BEST IF USED BY: 10/26/2013; TFMDAA290A, BEST IF USED BY: 10/27/2013; TFMDAA291A, BEST IF USED BY: 10/28/2013; TFMDAA295A, BEST IF USED BY: 11/01/2
best by10/27/2013/25/2013; TFMDAA289A, BEST IF USED BY: 10/26/2013; TFMDAA290A, BEST IF USED BY: 10/27/2013; TFMDAA291A, BEST IF USED BY: 10/28/2013; TFMDAA295A, BEST IF USED BY: 11/01/2013; TFMDAA296A, BEST IF USED BY: 11/02/2
best by10/28/2013/26/2013; TFMDAA290A, BEST IF USED BY: 10/27/2013; TFMDAA291A, BEST IF USED BY: 10/28/2013; TFMDAA295A, BEST IF USED BY: 11/01/2013; TFMDAA296A, BEST IF USED BY: 11/02/2013; TFMDAA297A, BEST IF USED BY: 11/03/2
best by11/01/2013/27/2013; TFMDAA291A, BEST IF USED BY: 10/28/2013; TFMDAA295A, BEST IF USED BY: 11/01/2013; TFMDAA296A, BEST IF USED BY: 11/02/2013; TFMDAA297A, BEST IF USED BY: 11/03/2013
best by11/02/2013/28/2013; TFMDAA295A, BEST IF USED BY: 11/01/2013; TFMDAA296A, BEST IF USED BY: 11/02/2013; TFMDAA297A, BEST IF USED BY: 11/03/2013
best by11/03/2013/01/2013; TFMDAA296A, BEST IF USED BY: 11/02/2013; TFMDAA297A, BEST IF USED BY: 11/03/2013

Recall details

Recall number
F-0398-2014
Event ID
66709
FDA status
Terminated
Initiated
Oct 25, 2013
Reported
Jan 1, 2014
Classified
Dec 23, 2013
Terminated
Feb 7, 2014
Quantity
240 units
Location
Jessup, MD, 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

NY, NJ, PA, MA, MO, MA

FDA source record · F-0398-2014

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

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