Teva recalls 1 mg Prazosin capsules due to potential carcinogenic impurities. Affected lots have NDC 0093-4067-01 or 10. Stop using if you have these specific 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 1 mg Prazosin capsules that may contain harmful levels of N-nitroso Prazosin impurities. This impurity could potentially increase cancer risk, so affected users should stop using the product.
The product contains N-nitroso Prazosin impurities at levels above safety limits. These impurities are linked to potential cancer risk, but the recall does not indicate immediate health threats.
People with prescriptions for 1 mg Prazosin capsules from Teva Pharmaceuticals. Those who have the specific lot numbers listed in the recall are most at risk.
Check your capsule packaging for NDC 0093-4067-01 (100 capsules) or 0093-4067-10 (1000 capsules). Look for specific lot numbers and expiration dates listed in the recall.
Review your capsule packaging for NDC numbers 0093-4067-01 or 0093-4067-10 and associated lot numbers.
The recall indicates potential carcinogenic impurities, but the product is not considered immediately dangerous. Affected users should stop using it.
Check your product details against the recall list. If you have the specific NDC and lot numbers, stop using it immediately.
Look for NDC 0093-4067-01 (100 capsules) or 0093-4067-10 (1000 capsules) with the listed lot numbers and expiration dates.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0104-2026 — Teva Teva Hello, I own a Teva that is covered by recall D-0104-2026 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.
