Cardinal Healthcare recalls estradiol tablets due to potential temperature exposure during storage. This may affect product stability and safety. Learn if your tablets are affected and what to do.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling estradiol tablets that may have been exposed to temperatures outside their labeled storage conditions. This could affect the tablets' stability and safety, though the recall does not specify a risk of serious injury.
The tablets were exposed to temperatures outside their labeled storage conditions during manufacturing. This could potentially affect the product's stability and safety, though the recall does not specify a risk of serious injury.
People who have estradiol tablets labeled as 0.5mg, 100 tablets, for treatment use. Those most at risk are individuals taking hormone therapy who rely on these specific tablets.
Check for the product name 'Estradiol Tablets USP, 0.5MG 100 Tablets, Tx Only' with manufacturer 'Teva Pharmaceuticals USA, Inc.' and NDC code 0555-0899-02, batch 100023687.
Look for the NDC code 0555-0899-02 and batch number 100023687 on the product label.
The recall states the tablets may have been exposed to temperatures outside labeled storage conditions, which could affect stability and safety, but it does not specify a risk of serious injury.
Check for the NDC code 0555-0899-02 and batch number 100023687 on the product label.
The recall does not provide a specific remedy, so contact Cardinal Healthcare for guidance.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0180-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0180-2024 from Cardinal Healthcare. 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.
