Check the Batch
Class IITerminated in FDA datasetRecall initiated Jul 23, 2012

6" Club Sandwich, 8" Club Sandwich, Club Sandwich Triangle, and Wide Wedge Club Sandwich

Recalling firm: Rita's Fine Food, Inc. Dba Da Vinci's

Why it was recalled

The recall was initiated because Rita's Fine Food sandwiches have undeclared milk as a sub-ingredient in cheese.

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: Jan 23, 2013.

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

Product6" Club Sandwich, 8" Club Sandwich, Club Sandwich Triangle, and Wide Wedge Club Sandwich
UPC697436000058, 697436000355, 697436000928, 697436001437

FDA code information

UPC 697436000058 (6" size); UPC 697436000355 (8" size); UPC 697436000928 (triangle); UPC 697436001437 (wide wedge).

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

Full FDA record and distribution details

Original product description

6" Club Sandwich, 8" Club Sandwich, Club Sandwich Triangle, and Wide Wedge Club Sandwich

Extracted codes and context

TypeCode / valueContext
UPC697436000058UPC 697436000058 (6" size); UPC 697436000355 (8" size); UPC 697436000928 (triangle); UPC 697436001437 (wide wedge).
UPC697436000355UPC 697436000058 (6" size); UPC 697436000355 (8" size); UPC 697436000928 (triangle); UPC 697436001437 (wide wedge).
UPC697436000928UPC 697436000058 (6" size); UPC 697436000355 (8" size); UPC 697436000928 (triangle); UPC 697436001437 (wide wedge).
UPC6974360014370058 (6" size); UPC 697436000355 (8" size); UPC 697436000928 (triangle); UPC 697436001437 (wide wedge).

Original FDA recall reason

The recall was initiated because Rita's Fine Food sandwiches have undeclared milk as a sub-ingredient in cheese.

Recall details

Recall number
F-2018-2012
Event ID
62692
FDA status
Terminated
Initiated
Jul 23, 2012
Reported
Sep 5, 2012
Classified
Aug 24, 2012
Terminated
Jan 23, 2013
Quantity
430 units total
Location
La Mesa, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

CA

FDA source record · F-2018-2012

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

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