Cardinal Healthcare recalls 80mg Terconazole vaginal suppositories with applicator due to temperature exposure during storage. This may affect product stability and safety.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling 80mg Terconazole vaginal suppositories with applicator because they were exposed to temperatures outside the labeled storage conditions. This could potentially affect product stability and safety.
The products were exposed to temperatures outside the labeled storage conditions during manufacturing. This could potentially affect the product's stability and safety, though the exact risk level is not specified in the recall.
People with prescriptions for Terconazole vaginal suppositories who purchased these products from pharmacies or online. Those with specific storage conditions for the medication may be at higher risk.
Check for the product name 'Terconazole Vaginal Suppositories, 80 mg, 3 Suppositories with Vaginal Applicator' and the NDC number 0713-0552-73. Products manufactured by Cosette Pharmaceuticals, Inc. with batch number 1014228A are affected.
Verify the product name, NDC number 0713-0552-73, and batch number 1014228A to confirm if your product is recalled.
The recall states the products were exposed to temperatures outside labeled storage conditions, which could affect stability and safety, but specific safety risks are not detailed.
Check for the product name 'Terconazole Vaginal Suppositories, 80 mg, 3 Suppositories with Vaginal Applicator', NDC number 0713-0552-73, and batch number 1014228A.
The recall does not specify a remedy, so you should check with your pharmacist or healthcare provider 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-0198-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0198-2024 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.
