Sentara recalls methylprednisolone 12mg in 1.2ml syringes due to lack of sterility assurance. This steroid injection may cause infection if used after the expiration date of December 29-31, 2022.
Lack of sterility assurance
Sentara is recalling methylprednisolone 12mg in 1.2ml syringes because they lack sterility assurance. This could lead to infections if the syringe is used after the expiration date of December 29-31, 2022.
The syringes do not have proper sterility assurance, meaning they could be contaminated with bacteria. If used after the expiration date, this increases the risk of infection in patients receiving the injection.
Patients receiving methylprednisolone injections through Sentara Home Infusion Pharmacy Services. Those using syringes beyond the expiration date of December 29-31, 2022 are at higher risk.
Check for the product name 'Methylprednisolone 12MG IN NS 1.2ML SYRINGE' and the expiration date of December 29-31, 2022. This product was sold by Sentara Home Infusion Pharmacy Services in Chesapeake, VA.
Verify the expiration date on the syringe; if it's after December 29-31, 2022, it may be unsafe.
The product may not be sterile and could cause infection if used after the expiration date of December 29-31, 2022.
Look for the product name 'Methylprednisolone 12MG IN NS 1.2ML SYRINGE' with an expiration date of December 29-31, 2022.
Check the expiration date; if it's after December 29-31, 2022, do not use it and contact your healthcare provider.
We’ve drafted a message you can send Sentara to request your refund or repair — edit it as you like.
Subject: Recall D-0305-2023 — Sentara Sentara Hello, I own a Sentara that is covered by recall D-0305-2023 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.
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.