Sentara Infusion Services recalls specific TPN products due to lack of sterility assurance. These products were sold with a beyond-use date of December 24-31, 2022. Consumers should check their product labels for the listed formulations.
Lack of sterility assurance
Sentara Infusion Services has recalled several types of TPN (total parenteral nutrition) products because they may not be sterile. This could lead to infections if used improperly. The products were sold with a beyond-use date of December 24-31, 2022.
TPN products are critical medications for patients who cannot eat normally. Lack of sterility assurance means the products could become contaminated, leading to serious infections if used.
Patients receiving TPN therapy through Sentara Home Infusion Pharmacy Services are most at risk. The affected products were sold with a beyond-use date of December 24-31, 2022.
Check the product label for the specific TPN formulations listed: (a) 115GM/AA, 215GM/DEX, 25GM/LIP 1150ML; (b) 90GM/AA, 215GM/DEX, 25GM/LIP 1150ML; (c) TPN AA: 100GM DEX: 105GM 2700ML; and others as detailed in the recall notice. The products were sold with a beyond-use date of December 24-31, 2022.
Look for the specific TPN formulations listed in the recall notice to confirm if your product is affected.
The affected products include TPN formulations (a) 115GM/AA, 215GM/DEX, 25GM/LIP 1150ML; (b) 90GM/AA, 215GM/DEX, 25GM/LIP 1150ML; (c) TPN AA: 100GM DEX: 105GM 2700ML; and others as detailed in the recall notice.
The products were sold with a beyond-use date of December 24-31, 2022.
Check the product label for the specific formulations listed in the recall notice. The products were sold with a beyond-use date of 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-0320-2023 — Sentara Infusion Services Sentara Infusion Services Hello, I own a Sentara Infusion Services that is covered by recall D-0320-2023 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.
