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RECALL RECORD — CLASS IIRecall closedF-1012-2022/FDA enforcement
The Procter & Gamble Company·Food·Mar 24, 2022

Align Digestive De-stress Capsules 21ct Bottle Packaged in Paper Carton 12 Cartons Per Case

What you need to know

Class II

  • What happened

    Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 FDADistribution not listedMore food

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Product identification

Source: FDA FOOD

Brand nameThe Procter & Gamble Company
Recalling firmThe Procter & Gamble CompanyCincinnati, OH, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot No. 1022171991 Product No. 80347747 Best By Date: 07/31/2022
Distribution area

Product was sent to a 3rd party for destruction due to not meeting micro specs

United States

Quantity affected23, 928 cartons
Recall initiationFDA report date: May 4, 2022
FDA recall numberF-1012-2022

Beyond the headline

The recall, in context

The Procter & Gamble Company initiated this food recall on March 24, 2022. The FDA enforcement report states: Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store. The FDA report lists distribution as: Product was sent to a 3rd party for destruction due to not meeting micro specs.

The FDA enforcement report describes the reason as: Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.

Align Digestive De-stress Capsules 21ct Bottle Packaged in Paper Carton 12 Cartons Per Case was made or distributed by The Procter & Gamble Company in Cincinnati, OH, United States. This page reflects FDA report F-1012-2022, dated May 4, 2022.

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, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

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

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 Align Digestive De-stress Capsules 21ct Bottle Packaged in Paper Carton 12 Cartons Per Case recall?

The Procter & Gamble Company recalled Align Digestive De-stress Capsules 21ct Bottle Packaged in Paper Carton 12 Cartons Per Case in an FDA Class II enforcement action reported as F-1012-2022. Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.

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.

Is the The Procter & Gamble Company 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-1012-2022. 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.