Sentara recalls IMIPENEM/CILASTATIN 2000MG in NS 400ML (NDC 63323-0322-25) due to lack of sterility assurance. This antibiotic, used with Curlin pumps, may cause infections if not properly sterilized.
Lack of sterility assurance
Sentara is recalling a specific antibiotic solution that can cause infections if not properly sterilized. This recall affects patients using the product with Curlin pumps and requires immediate action to prevent infection risks.
The solution lacks sterility assurance, meaning it could become contaminated and cause infections when administered. This is a critical issue for patients who rely on this medication for treatment.
Patients receiving this antibiotic through home infusion therapy using Curlin pumps are most at risk. The product was sold with a specific NDC number and expiration date.
Check for the NDC number 63323-0322-25 on the product label. The product was sold by Sentara Home Infusion Pharmacy with an expiration date of December 25-30, 2022.
Look for the NDC number 63323-0322-25 on the product label.
The recall states there is a lack of sterility assurance, which could lead to infections. Do not use this product.
The product expires December 25-30, 2022.
The recall record does not specify a replacement process.
We’ve drafted a message you can send Sentara to request your refund or repair — edit it as you like.
Subject: Recall D-0297-2023 — Sentara Sentara Hello, I own a Sentara that is covered by recall D-0297-2023 from Sentara. 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.
