Cardinal Healthcare recalls Lillow birth control pills due to potential temperature exposure during storage. This may affect product stability and safety. Learn if your pills are affected and what to do.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling Lillow birth control pills that may have been exposed to temperatures outside the labeled storage conditions. This could affect the pills' stability and safety, so affected users should stop using them and contact their healthcare provider.
The pills may have been exposed to temperatures outside the labeled storage conditions during manufacturing or distribution. This could potentially affect the stability of the medication, though the risk of serious harm is low.
People who have the Lillow birth control pills (0.15 mg/0.03 mg, 28-tablet blister pack) prescribed by a doctor. Women using this specific birth control method are most at risk.
Check for the Lillow birth control pills (0.15 mg/0.03 mg, 28-tablet blister pack) with NDC code 69238-1554-6 and batch number A5921. These pills are prescription-only and distributed by Amneal Pharmaceuticals.
If you have the recalled Lillow birth control pills, stop using them immediately.
Talk to your doctor or healthcare provider about alternative birth control options.
The recall is due to potential temperature exposure, which may affect stability. The manufacturer recommends stopping use and consulting a healthcare provider.
Look for the NDC code 69238-1554-6 and batch number A5921 on the blister pack. These pills are prescription-only.
Stop using them immediately and contact your healthcare provider for alternative birth control options.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0187-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0187-2024 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.
