Sentara recalls KYTRIL 350mcg in 3.5ml NS syringes due to lack of sterility assurance. This could lead to infections if used improperly. Check your medication's expiration date and contact Sentara for details.
Lack of sterility assurance
Sentara is recalling KYTRIL 350mcg in 3.5ml NS syringes because they lack sterility assurance. This could cause infections if the syringe is used without proper cleaning. The recall covers syringes with a December 29, 2022 expiration date.
The syringes do not have adequate sterility assurance, meaning they could become contaminated. If used without proper cleaning, this could lead to infections. The risk is low because the syringes are for medical use and the issue is related to sterility, not immediate harm.
People who have received KYTRIL 350mcg in 3.5ml NS syringes from Sentara Home Infusion Pharmacy Services. Those using the syringes for medical purposes are most at risk.
Check for KYTRIL 350mcg in 3.5ml NS syringes with a December 29, 2022 expiration date. These were sold by Sentara Home Infusion Pharmacy Services in Chesapeake, VA.
Look for the expiration date on the syringe, which should be December 29, 2022 or earlier.
The recall states there is a lack of sterility assurance, so it is not safe to use without proper cleaning. However, the risk is low as the syringes are for medical use.
Check for KYTRIL 350mcg in 3.5ml NS syringes with a December 29, 2022 expiration date sold by Sentara Home Infusion Pharmacy Services.
The recall does not specify a remedy, so contact Sentara Home Infusion Pharmacy Services for further instructions.
We’ve drafted a message you can send Sentara to request your refund or repair — edit it as you like.
Subject: Recall D-0299-2023 — Sentara Sentara Hello, I own a Sentara that is covered by recall D-0299-2023 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.
