Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Anagrelide Capsules USP Recalled by Teva Pharmaceuticals USA Inc Due to Failed Dissolution Specifications- Low Out-Of-Specification results obtained during...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Teva Pharmaceuticals USA Inc directly.
Affected Products
Anagrelide Capsules USP, 0.5 mg, 100-count bottles, Rx Only, Manufactured in India For: TEVA PHARMACEUTICALS USA, Inc., North Wales, PA 19454. NDC 0172-5241-60.
Quantity: 4224 cartons
Why Was This Recalled?
Failed Dissolution Specifications- Low Out-Of-Specification results obtained during stability testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teva Pharmaceuticals USA Inc
Teva Pharmaceuticals USA Inc has 20 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report