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RECALL RECORD — CLASS IIRecall closedF-0786-2016/FDA enforcement
Nestle USA·Food·Mar 10, 2016

Digiorno Thin & Crispy Spinach and Garlic Pizza

What you need to know

Class II

  • What happened

    Nestle is recalling a limited number of DiGiorno, Lean Cuisine, and Stouffer's products due to the potential presence of glass pieces.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Glass fragments can cause cuts, choking or internal injury if swallowed.

  • 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 FDANationwide (US)More food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameNestle USA
Recalling firmNestle USASolon, OH, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Production code: 5363525921, 5363525922, 5364525921. Best Before: July 2016 Production code: 6019525921, 6019525922. Best Before: Aug 2016
Distribution area
Nationwide

Nationwide

United States

Quantity affected21, 997 cases
Recall initiationFDA report date: March 30, 2016
FDA recall numberF-0786-2016

Beyond the headline

The recall, in context

Nestle USA initiated this food recall on March 10, 2016. The FDA enforcement report states: Nestle is recalling a limited number of DiGiorno, Lean Cuisine, and Stouffer's products due to the potential presence of glass pieces. The FDA report lists distribution as: Nationwide.

The FDA enforcement report describes the reason as: Nestle is recalling a limited number of DiGiorno, Lean Cuisine, and Stouffer's products due to the potential presence of glass pieces.

Digiorno Thin & Crispy Spinach and Garlic Pizza was made or distributed by Nestle USA in Solon, OH, United States. This page reflects FDA report F-0786-2016, dated March 30, 2016.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, glass fragments can cause cuts, choking or internal injury if swallowed.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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

Glass contamination

Possible health effects

Glass fragments can cause cuts to the mouth, throat or digestive tract. Do not inspect or taste a suspect product.

Higher-risk groups

Children, older adults and anyone who may swallow a fragment without noticing are at greater risk of injury.

What to do now

  1. 1Stop eating or using the product and do not attempt to remove fragments by tasting it.
  2. 2Seek medical care if anyone has swallowed glass, has throat or abdominal pain, or is vomiting blood.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund; follow the recall notice for disposal.

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 Digiorno Thin & Crispy Spinach and Garlic Pizza recall?

Nestle USA recalled Digiorno Thin & Crispy Spinach and Garlic Pizza in an FDA Class II enforcement action reported as F-0786-2016. Nestle is recalling a limited number of DiGiorno, Lean Cuisine, and Stouffer's products due to the potential presence of glass pieces.

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 eating or using the product and do not attempt to remove fragments by tasting it. Seek medical care if anyone has swallowed glass, has throat or abdominal pain, or is vomiting blood. Keep the packaging and contact the retailer or manufacturer about a refund; follow the recall notice for disposal.

Is the Nestle USA 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-0786-2016. 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

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