Teva recalls Nortrel 0.5/35 tablets with discolored (blue) tablets mixed in. Affected units have specific NDC and lot numbers. Stop using if you see discoloration.
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
Teva is recalling Nortrel 0.5/35 tablets that may contain discolored blue tablets. This could be a safety issue if the discolored tablets are taken, though the recall doesn't specify a risk of injury.
Discolored tablets (shades of blue) mixed with white tablets could be a sign of contamination. Taking these discolored tablets might lead to unintended side effects, but the recall does not specify a risk of serious injury.
People who have the Nortrel 0.5/35 tablets with lot number 100042978 (expiring July 31, 2024) are affected. Women using this birth control medication are most at risk.
Check for blue or discolored tablets in the carton. The affected product has NDC 0555-9008-67 and lot number 100042978, expiring July 31, 2024.
Look for blue or discolored tablets mixed with white tablets in the carton.
The recall does not specify a risk of serious injury. The hazard is discolored tablets, but the exact risk is not described.
Check for NDC 0555-9008-67 and lot number 100042978 on the carton. The product expires July 31, 2024.
The recall does not specify a remedy. You should check with your doctor or pharmacist for advice.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0321-2024 — Teva Teva Hello, I own a Teva that is covered by recall D-0321-2024 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.
