RemedyRePack recalls Cefixime 400mg capsules with failed impurities/degradation specs. Rx-only products from specific lots and NDCs may pose safety risks.
Failed Impurities/Degradation Specifications
RemedyRePack is recalling certain Cefixime 400 mg capsules due to failed impurities or degradation specifications. This could potentially lead to unsafe drug content in the medication.
The capsules may contain impurities or have degraded beyond safe levels, which could affect the medication's safety and effectiveness. This issue occurs in specific batches with particular lot numbers and expiration dates.
Prescription holders of the specific Cefixime 400 mg capsules with the listed NDC numbers and lot codes are affected. Patients taking these medications should be cautious.
Check for the product name 'Cefixime 400 mg capsule' with NDC numbers 70518-2749-02 or 70518-2749-03. Look for specific lot numbers and expiration dates listed in the recall notice.
Verify your capsule's NDC number and lot code against the list provided in the recall notice.
The recall indicates potential impurities or degradation, so it is not safe to use without checking the specific lot numbers and NDCs listed in the recall.
The recall does not specify a remedy, so you should check the product details and contact your healthcare provider for guidance.
Check the NDC number (70518-2749-02 or 70518-2749-03) and lot code against the list provided in the recall notice.
We’ve drafted a message you can send RemedyRePack to request your refund or repair — edit it as you like.
Subject: Recall D-0360-2022 — RemedyRePack RemedyRePack Hello, I own a RemedyRePack that is covered by recall D-0360-2022 from RemedyRePack. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
