Align Digestive De-Stress Capsules 21ct bottle packaged in paper carton 12 cartons per case
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1012-2022.
Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1012-2022.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact The Procter & Gamble Company or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1012-2022.
The Procter & Gamble Company
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
The Procter & Gamble Company Recall FAQ
The Procter & Gamble Company is the subject of a food safety report: Align Digestive De-Stress Capsules 21ct bottle packaged in paper carton 12 cartons per case. The notice was published on March 24, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 23,928 units are potentially affected.