VerifyRecall
Alerts
RECALL RECORD — CLASS IIIRecall closedF-0006-2018/FDA enforcement
Quickie Stores, INC.·Food·Sep 21, 2017

Tofustrami Sofu Sandwich, Plum Bistro 2go Brand, Packaged in a Transparent Plastic Clamshell…

What you need to know

Class III

  • What happened

    Sandwiches are recalled due to undeclared wheat.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDAIN, WAMore food

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Share via WhatsApp

Match before you discard

Product identification

Source: FDA FOOD

Brand nameQuickie Stores, INC.
Recalling firmQuickie Stores, INC.Tacoma, WA, United States
UPC / barcodes
8 64801 00010 8
Lot / date codes
  • Expiration dates or best-by dates: 9/17 and 09/24.
Distribution area
INWA

distributed in WA only

United States

Quantity affected50 packages
Recall initiationFDA report date: October 11, 2017
FDA recall numberF-0006-2018

Beyond the headline

The recall, in context

Quickie Stores, INC. initiated this food recall on September 21, 2017. The FDA enforcement report states: Sandwiches are recalled due to undeclared wheat. The FDA report lists distribution as: distributed in WA only.

The FDA enforcement report describes the reason as: Sandwiches are recalled due to undeclared wheat.

Tofustrami Sofu Sandwich, Plum Bistro 2go Brand, Packaged in a Transparent Plastic Clamshell… was made or distributed by Quickie Stores, INC. in Tacoma, WA, United States. This page reflects FDA report F-0006-2018, dated October 11, 2017.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared wheat or gluten

Symptoms to watch for

Wheat allergy can cause hives, nausea, cramps, breathing difficulty or anaphylaxis. For celiac disease, even small amounts of gluten can cause intestinal damage.

When symptoms may appear

Allergic reactions can begin within minutes to hours. Celiac-related intestinal effects may be delayed.

Higher-risk groups

People with wheat allergy, celiac disease, non-celiac gluten sensitivity or a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a wheat allergy or must avoid gluten.
  2. 2Seek emergency care for breathing difficulty or other signs of a severe allergic reaction.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Tofustrami Sofu Sandwich, Plum Bistro 2go Brand, Packaged in a Transparent Plastic Clamshell… recall?

Quickie Stores, INC. recalled Tofustrami Sofu Sandwich, Plum Bistro 2go Brand, Packaged in a Transparent Plastic Clamshell… in an FDA Class III enforcement action reported as F-0006-2018. Sandwiches are recalled due to undeclared wheat.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a wheat allergy or must avoid gluten. Seek emergency care for breathing difficulty or other signs of a severe allergic reaction. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Quickie Stores, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0006-2018. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Quickie Stores, INC.

View brand
Class III·

Quickie Stores, INC.

Southern Bbq Tofu Sandwich, Plum Bistro 2go Brand, Packaged in a Transparent Plastic Clamshell…

Sandwiches are recalled due to undeclared wheat.

IN, WAFood
Class III·

Quickie Stores, INC.

New York Deli Tempeh Sandwich, Plum Bistro 2go Brand, Packaged in a Transparent Plastic…

Sandwiches are recalled due to undeclared wheat.

IN, WAFood

Related alerts

Recent Undeclared allergens recalls

All alerts
Class I·

Oliva on Main

Riad's Oliva to Go Spicy Baba Ghanouj

Contains undeclared sesame

MA, CTFood
Class I·

Oliva on Main

Riad's Oliva to Go Baba Ghanouj

Contains undeclared sesame

MA, CTFood

Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.