Class IIITerminated in FDA datasetRecall initiated Sep 21, 2017

New York Deli tempeh sandwich, plum bistro 2go brand, packaged in a transparent plastic…

Recalling firm: Quickie Stores, Inc.

Why it was recalled

Sandwiches are recalled due to undeclared wheat.

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: Dec 18, 2017.

Check your package

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

ProductNew York Deli tempeh sandwich, plum bistro 2go brand, packaged in a transparent plastic clamshell container, sold at 10 oz. or 12 oz. UPC 8 64801 00010 8. The label is read in parts: "***NEW YORK DELI tempeh sandwich***plum bistro 2go***Sold by Quickie Stores Inc. 1324 M.L.K. Jr Way, Tacoma, WA 98405***.
Package size10 oz
UPC864801000108

FDA code information

Expiration dates or best-by dates: 9/17 and 9/24.

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

Full FDA record and distribution details

Original product description

New York Deli tempeh sandwich, plum bistro 2go brand, packaged in a transparent plastic clamshell container, sold at 10 oz. or 12 oz. UPC 8 64801 00010 8. The label is read in parts: "***NEW YORK DELI tempeh sandwich***plum bistro 2go***Sold by Quickie Stores Inc. 1324 M.L.K. Jr Way, Tacoma, WA 98405***.

Extracted codes and context

TypeCode / valueContext
UPC864801000108aged in a transparent plastic clamshell container, sold at 10 oz. or 12 oz. UPC 8 64801 00010 8. The label is read in parts: "***NEW YORK DELI tempeh sandwich***plum bistro 2go***Sold by Quickie Stores Inc. 1324

Original FDA recall reason

Sandwiches are recalled due to undeclared wheat.

Recall details

Recall number
F-0008-2018
Event ID
78160
FDA status
Terminated
Initiated
Sep 21, 2017
Reported
Oct 11, 2017
Classified
Oct 3, 2017
Terminated
Dec 18, 2017
Quantity
50 packages
Location
Tacoma, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Visit

Where it was distributed

distributed in WA only

FDA source record · F-0008-2018

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

Follow official FDA and manufacturer guidance.