Demonstration record. This is sample data used to show the page structure. It is not a real recall and must not be acted on.
Verified recall information
Blood Pressure Tablets 10mg recall
Certain lots of a blood pressure medication are being recalled because they may contain an impurity above the acceptable limit.
- Agency
- FDA — U.S. Food and Drug Administration
- Recall number
- DEMO-FDA-0001
- Recall date
- August 17, 2026
- Last updated
- August 17, 2026
- Company
- DemoPharma Laboratories
- Classification
- Class II
What was recalled?
10mg blood pressure tablets in 30-count and 90-count bottles.
Brand: DemoPharma
Why was it recalled?
Testing found an impurity above the acceptable intake limit in specific lots.
Hazard: Impurity above acceptable limit
Long-term exposure above the acceptable limit may pose a health risk.
How do I know if I have it?
Check the lot number DP-4471 or DP-4472 on the bottle label.
- Lot / batch codes
- DP-4471, DP-4472
- Units affected
- About 9,300 bottles
What should I do?
Do not stop taking your medication before talking to your pharmacist or doctor about a replacement.
Remedy: Contact the pharmacy for a replacement supply.
Company contact: DemoPharma, 800-555-0133
Where was it sold or distributed?
Distributed nationwide.
Sold at: Retail pharmacies
Official source
U.S. Food and Drug Administration issued this recall. Always confirm details with the agency.
View original government recall