Teva recalls Nortrel 7/7/7 tablets with discoloration (blue shades) mixed in with white tablets. Discarded tablets may be unsafe. Check NDC 0555-9012-58 and lot 100040731 for affected units.
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
Teva is recalling Nortrel 7/7/7 birth control tablets that may have blue discoloration mixed with white tablets. This could mean some tablets are unsafe to take. Affected units have NDC 0555-9012-58 and lot number 100040731.
Discolored tablets (blue shades) may be mixed with white tablets in the package. This could mean some tablets are unsafe to take, but the hazard is not described as causing serious injury.
Women who have been prescribed Nortrel 7/7/7 birth control tablets with NDC 0555-9012-58 and lot 100040731 are affected. Those who take the tablets as directed are most at risk.
Check for blue discoloration in the tablets. Affected units have NDC 0555-9012-58 and lot number 100040731.
Look for blue shades mixed with white tablets in the package.
The recall states discoloration may be present but does not describe specific safety risks.
Check for NDC 0555-9012-58 and lot number 100040731 on the packaging.
The recall does not specify a remedy, so no action is required beyond checking for discoloration.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0322-2024 — Teva Teva Hello, I own a Teva that is covered by recall D-0322-2024 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.
