Sentara Infusion Services recalls specific Milrinone doses due to lack of sterility assurance. These products may cause infections if used improperly.
Lack of sterility assurance
Sentara Infusion Services is recalling specific Milrinone doses that lack sterility assurance. Using these products could lead to infections, especially in medical settings where sterile conditions are critical.
The products lack sterility assurance, meaning they may contain contaminants that could cause infections. This is a critical issue for medical use where sterile solutions are required to prevent complications.
Patients receiving Milrinone injections through Sentara Home Infusion Pharmacy Services in the U.S. are most at risk, particularly those with compromised immune systems.
Check for Milrinone doses labeled with specific concentrations (104MG-192MG in 0.45% NS) sold by Sentara Home Infusion Pharmacy Services. Products were distributed between December 24-31, 2022.
Look for the specific Milrinone doses listed in the recall notice, including concentrations like 104MG in 0.45% NS 130ML.
Reach out to Sentara Home Infusion Pharmacy Services at 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320 for assistance with the recall.
The products lack sterility assurance, which means they may contain contaminants that could cause infections.
Check the product label to see if it matches the recalled doses, then contact Sentara Home Infusion Pharmacy Services for guidance.
Yes, these products were distributed between December 24-31, 2022.
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-0307-2023 — Sentara Infusion Services Sentara Infusion Services Hello, I own a Sentara Infusion Services that is covered by recall D-0307-2023 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.
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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.
