Sentara Infusion Services recalls Lactated Ringers (1000ML, 2500ML, 3000ML, 3600ML, 500ML) due to lack of sterility assurance. These products were sold with a specific expiration date.
Lack of sterility assurance
Sentara Infusion Services is recalling certain Lactated Ringers IV fluids because they may not be sterile. This could lead to infections if used in medical treatments. Patients should check their product labels and contact the company if they have the recalled items.
The Lactated Ringers products lack sterility assurance, meaning they could contain harmful bacteria. If used in medical treatments, this could cause infections or other health issues.
Patients receiving IV hydration treatments through Sentara Home Infusion Pharmacy Services are most at risk. Healthcare providers using these products for medical purposes may also be affected.
Check for Lactated Ringers with volumes of 1000ML, 2500ML, 3000ML, 3600ML, or 500ML. The product has a National Drug Code (NDC) of 00338-0117-03 and was sold with a specific expiration date.
Look for the product volume and NDC code on the label to confirm if it matches the recalled items.
The product lacks sterility assurance, which could lead to infections if used in medical treatments.
The NDC code is 00338-0117-03.
Check the product label for volumes of 1000ML, 2500ML, 3000ML, 3600ML, or 500ML and the NDC code 00338-0117-03.
We’ve drafted a message you can send Sentara Infusion Services to request your refund or repair — edit it as you like.
Subject: Recall D-0300-2023 — Sentara Infusion Services Sentara Infusion Services Hello, I own a Sentara Infusion Services that is covered by recall D-0300-2023 from Sentara Infusion Services. 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.