FDA Recall United States Terminated Historical recordClass II
The Procter & Gamble Company
- Product
- Meta Psyllium Fiber Capsules packaged as 100 count or 160 co…
- Published
- February 28, 2024
- Distribution
- Alabama, Arizona, Arkansas, California,…
The Procter & Gamble Company Recall: Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.
United States
TerminatedClass II
- Company
- The Procter & Gamble Company
- Product
- Align Digestive De-Stress Capsules 21ct bottle packaged in…
- Recall date
- March 24, 2022
- Terminated
- September 8, 2022
- Source
- FDA
Reason for recall
Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Align Digestive De-Stress Capsules 21ct bottle packaged in paper carton 12 cartons per case | Not published in this source record | 23,928 cartons | Lot No. 1022171991 Product No. 80347747 Best By Date: 07/31/2022 |
Distribution
- Product was sent to a 3rd party for destruction due to not meeting micro specs
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1012-2022
- Event ID
- 89996
- Status
- Terminated
- Classification
- Class II
- Company
- The Procter & Gamble Company
- Product description
- Align Digestive De-Stress Capsules 21ct bottle packaged in paper carton 12 cartons per case
- Quantity
- 23,928 cartons
- Reason
- Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.
- Recall initiation date
- March 24, 2022
- Report date
- May 4, 2022
- Classification date
- Not published in this source record
- Termination date
- September 8, 2022
- Distribution pattern
- Product was sent to a 3rd party for destruction due to not meeting micro specs
- UPC, lot, and code information
- Lot No. 1022171991 Product No. 80347747 Best By Date: 07/31/2022
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: The Procter & Gamble Company
Other recalls from The Procter & Gamble Company
FDA Recall Terminated Historical recordClass II
Secret Dry Spray, Aluminum chlorohydrate 23.5%, Antiperspirant, Rose, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-380-10, UPC 0 37000 79884 2
- Published
- January 24, 2024
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Secret, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Lavender, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-383-10, UPC: 0 37000 72986 0
- Published
- January 24, 2024
- Distribution
- Nationwide
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
