Teva recalls Tri-Lo-Sprintec birth control tablets due to failed dissolution specifications. This may affect product effectiveness. Check NDC 0093-2140-62 and lot numbers for affected items.
Failed Dissolution Specifications
Teva is recalling Tri-Lo-Sprintec birth control tablets that failed dissolution specifications. This means the tablets might not work as intended, potentially affecting birth control effectiveness.
The tablets failed dissolution specifications, meaning they may not release hormones properly in the body. This could lead to reduced effectiveness in preventing pregnancy, but does not cause immediate injury or harm.
Women using Tri-Lo-Sprintec birth control tablets with NDC 0093-2140-62 and specific lot numbers are affected. Those who have been using the product without issues are at low risk.
Check for NDC 0093-2140-62 on the packaging. Affected lots include 100039678 (expiring 04/31/2024) and 100038111, 100042277 (expiring 07/31/2024).
Look for NDC 0093-2140-62 and lot numbers 100039678, 100038111, or 100042277 on the packaging.
The tablets failed dissolution specifications, which may affect their effectiveness in preventing pregnancy.
Check the product details to see if it's affected. If it is, contact Teva for guidance.
No, the recall is for potential reduced effectiveness, not a safety hazard that causes injury.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0428-2024 — Teva Teva Hello, I own a Teva that is covered by recall D-0428-2024 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.
