Sentara recalls specific TPN solutions due to lack of sterility assurance. These products were sold with a beyond-use date of December 25-31, 2022. Consumers should check their product labels for the listed formulations.
Lack of sterility assurance
Sentara is recalling certain TPN (total parenteral nutrition) products that lack sterility assurance. This means the products could be contaminated, posing a risk of infection if used. Affected products were sold with a beyond-use date of December 25-31, 2022.
The TPN products lack sterility assurance, meaning they could be contaminated with bacteria or other pathogens. If used, this could lead to serious infections, especially in patients who are immunocompromised or receiving critical care.
Patients receiving TPN treatments through Sentara Home Infusion Pharmacy Services are most at risk. These products were sold with a beyond-use date of December 25-31, 2022.
Check for the product labels that list the specific TPN formulations: (a) 95GM/AA, 385/DEX, 50GM/LIP 1800ML; (b) TPN AA:100GM DEX:250GM LIP:50GM 2400ML; or (c) TPN: AA 80GM; DEX 320GM; LIP 50GM in 2300ml. These products were sold with a beyond-use date of December 25-31, 2022.
Look for the specific TPN formulations listed in the recall notice to confirm if your product is affected.
Sentara is recalling specific TPN formulations: (a) 95GM/AA, 385/DEX, 50GM/LIP 1800ML; (b) TPN AA:100GM DEX:250GM LIP:50GM 2400ML; and (c) TPN: AA 80GM; DEX 320GM; LIP 50GM in 2300ml.
The products were sold with a beyond-use date of December 25-31, 2022.
Check your TPN product label for the specific formulations listed in the recall notice.
We’ve drafted a message you can send Sentara to request your refund or repair — edit it as you like.
Subject: Recall D-0321-2023 — Sentara Sentara Hello, I own a Sentara that is covered by recall D-0321-2023 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.
