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Unrated Food recall · FDA · Published March 24, 2022

Align Digestive De-Stress Capsules Recall: Micro Testing Failure

Procter & Gamble recalls Align Digestive De-Stress Capsules 21ct bottles due to micro testing failure. Product was sent for destruction but redirected for sale online. Consumers should check lot numbers and contact the company.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #F-1012-2022FoodProcter & Gamble ›
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Contact the company

Recalling firmThe Procter & Gamble Company1 Procter And Gamble Plz · Cincinnati, OH 45202-3315
✎ GovInfoNow plain-language explainer

Procter & Gamble is recalling Align Digestive De-Stress Capsules 21ct bottles because they failed micro testing. This means the product was sent for destruction but was redirected for sale online, posing a risk of contamination or improper quality. Read more at govinfonow.com/recall/13149-align-digestive-de-stress-capsules-recall-micro-testing-failure.

Source Summary by GovInfoNow · govinfonow.com/recall/13149-align-digestive-de-stress-capsules-recall-micro-testing-failure · Updated October 4, 2026 · FDA enforcement record: FDA #F-1012-2022

Cite this page

“Align Digestive De-Stress Capsules Recall: Micro Testing Failure.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13149-align-digestive-de-stress-capsules-recall-micro-testing-failure. Based on FDA recall #F-1012-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1012-2022%22&limit=1).

The FDA announced on March 24, 2022, that The Procter & Gamble Company voluntarily recalled Align Digestive De-Stress Capsules due to failed microbiological testing. The agency stated the product was redirected for sale through an online store instead of being destroyed.

How to tell if you have it

  • Brand: Procter & Gamble
  • Product: Align Digestive De-Stress Capsules 21ct bottle packaged in paper carton
  • Lot No.: 1022171991
  • Product No.: 80347747
  • Best By Date: 07/31/2022
  • Quantity: 23,928 cartons

The hazard

The product failed microbiological testing. The firm originally sent the product for destruction but was redirected to sell it through an online store.

Context

GovInfoNow's records show Procter & Gamble has four other recalls on record since November 23, 2021. Other recent recalls of similar products include Centric Compounding Recalls Tri-Immune Boost Due to Contamination (July 27, 2026), Imu-Tek Colostrum-5 Capsules Recall: Under-processed Risk (February 24, 2026), and Wellnov Joint Nourish Liquid Recall: Bacterial Contamination Risk (April 23, 2026).

How to tell if you have this one

Check for lot number 1022171991 and product number 80347747 on the bottle. The product was sold in 12 cartons per case with a best by date of 07/31/2022.

  • Brand
    Procter & Gamble
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for lot number 1022171991 and product number 80347747 on the bottle.

How this recall unfolded

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Mar 24, 202212. FDA classified it Class II: Apr 26, 202223. Published in FDA’s Enforcement Report: May 4, 202234. FDA terminated the recall: Sep 8, 202242022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1012-2022 (March 24, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1012-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA