Align Digestive De-Stress Capsules (Procter & Gamble) – micro testing failure (2022)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Align Digestive De-Stress Capsules 21ct bottle packaged in paper carton 12 cartons per case
Brand
The Procter & Gamble Company
Lot Codes / Batch Numbers
Lot No. 1022171991 Product No. 80347747 Best By Date: 07/31/2022
Products Sold
Lot No. 1022171991 Product No. 80347747 Best By Date: 07/31/2022
The Procter & Gamble Company is recalling Align Digestive De-Stress Capsules 21ct bottle packaged in paper carton 12 cartons per case due to Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026