Teva recalls 0.5mg Anagrelide Capsules due to failed dissolution testing. This may affect medication effectiveness. Check NDC 0172-5241-60 and lot # GD01090.
Failed Dissolution Specifications- Low Out-Of-Specification results obtained during stability testing.
Teva is recalling 0.5 mg Anagrel: 100-count capsules that failed dissolution testing. This could mean the medication doesn't work as intended, so affected users should contact their doctor.
The capsules failed dissolution testing, meaning they may not release the medication properly. This could lead to the drug not working as intended, but it does not cause immediate harm.
People with a prescription for Anagrelide Capsules 0.5 mg, 100-count bottles. Those who have the specific lot number GD01090 are most at risk.
Check for the NDC code 0172-5241-60 and lot number GD01090 on the bottle. The product is a prescription-only 0.5 mg capsule.
Look for the NDC code 0172-5241-60 and lot number GD01090 on the bottle.
The recall is due to failed dissolution testing, which may affect medication effectiveness. Consult your doctor if you have the recalled product.
Check for NDC code 0172-5241-60 and lot number GD01090 on the bottle.
Contact your doctor to discuss alternatives, as the product may not work as intended.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0992-2022 — Teva Teva Hello, I own a Teva that is covered by recall D-0992-2022 from Teva. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
