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RECALL RECORD — CLASS IIIRecall closedF-0142-2018/FDA enforcement
Blue Line Food Service Distribution·Food·Oct 5, 2017

Deep Dish Pre Mix Dough

What you need to know

Class III

  • What happened

    Blue Line Distribution is voluntarily recalling certain pre-mix parbake dough mix products due to the possible presence of pieces of plastic pen, which have been found in…

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAMIMore food

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Product identification

Source: FDA FOOD

Brand nameBlue Line Food Service Distribution
Recalling firmBlue Line Food Service DistributionFarmington Hills, MI, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Deep Dish pre mix dough, Batches, Lot & Date Codes: Batch 237, 07/24/2017
  • Batch 689, 07/25/2017
  • Batch 693, 07/25/2017.
Distribution area
MI

Domestic: MI only

United States

Quantity affected2011 lbs., 2005 lbs., 2062 lbs.
Recall initiationFDA report date: November 15, 2017
FDA recall numberF-0142-2018

Beyond the headline

The recall, in context

Blue Line Food Service Distribution initiated this food recall on October 5, 2017. The FDA enforcement report states: Blue Line Distribution is voluntarily recalling certain pre-mix parbake dough mix products due to the possible presence of pieces of plastic pen, which have been found in certain batches of the pre-mix. The FDA report lists distribution as: Domestic: MI only.

The FDA enforcement report describes the reason as: Blue Line Distribution is voluntarily recalling certain pre-mix parbake dough mix products due to the possible presence of pieces of plastic pen, which have been found in certain batches of the pre-mix.

Deep Dish Pre Mix Dough was made or distributed by Blue Line Food Service Distribution in Farmington Hills, MI, United States. This page reflects FDA report F-0142-2018, dated November 15, 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, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

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 lot and date codes 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

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

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 Deep Dish Pre Mix Dough recall?

Blue Line Food Service Distribution recalled Deep Dish Pre Mix Dough in an FDA Class III enforcement action reported as F-0142-2018. Blue Line Distribution is voluntarily recalling certain pre-mix parbake dough mix products due to the possible presence of pieces of plastic pen, which have been found in…

What are the symptoms of Product safety recall exposure?

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Who is most at risk from Product safety recall?

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

How do I get a refund from Blue Line Food Service Distribution?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0142-2018 and keep the packaging, lot code and proof of purchase if you have them.

Is the Blue Line Food Service Distribution 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-0142-2018. 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

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