Teva Pharmaceuticals recalls 2mg Prazosin capsules with N-nitroso impurity levels above safety limits. Consumers should check NDC numbers and expiration dates for affected lots.
CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.
Teva Pharmaceuticals is recalling 2mg Prazosin capsules due to test results showing N-nitroso Prazosin impurities above safe levels. This impurity could potentially increase cancer risk with long-term use.
The test results show N-nitroso Prazosin impurities in the capsules that exceed the acceptable safety limits. This impurity is classified as a potential carcinogen, meaning it could increase cancer risk with long-term use of the product.
People with prescriptions for 2mg Prazosin capsules from Teva Pharmaceuticals. Those who have the specific NDC numbers and expiration dates listed in the recall are most at risk.
Check for NDC numbers 0093-4068-01 or 0093-4068-10 on the packaging. The affected lots have specific expiration dates listed in the recall notice.
Look for NDC numbers 0093-4068-01 or 0093-4068-10 on the capsule packaging.
The recall states that test results for N-nitroso Prazosin impurity are above acceptable safety limits, so the product is not safe for long-term use.
The recall does not specify a remedy, so contact your healthcare provider for guidance on whether to stop using the product.
Check the NDC numbers on the packaging: 0093-4068-01 or 0093-4068-10, and verify the expiration date against the list provided in the recall.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0105-2026 — Teva Teva Hello, I own a Teva that is covered by recall D-0105-2026 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.
