Pharmacy Plus, Inc. dba Vital Care Compounder recalls specific medication vials for potential contamination. Products may not be sterile as found in FDA inspections. Consumers should check lot numbers and contact the company for details.
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Vital Care Compounder has recalled certain medication vials that may not be sterile, as found in FDA inspections. Using these vials could lead to infections or other health risks if the medication is not properly sterile.
FDA inspections found the vials were produced without sufficient assurance of sterility. This means the medication could be contaminated, potentially causing infections or other health issues if used.
Prescription medication users who purchased the recalled vials from pharmacies or clinics. Those with medical conditions requiring these medications are at higher risk.
Check for lot numbers 64409 (bought by 04/08/2023) or 60849 (bought by 05/23/2023) on the vial packaging. The product is a prescription-only solution for specific medical uses.
Look for lot numbers 64409 or 60849 on the vial packaging to confirm if it is part of the recall.
FDA inspections found the vials were produced without sufficient assurance of sterility, meaning they may not be safe for use.
Check the lot number on the vial packaging; the recalled lots are 64409 (bought by 04/08/2023) or 60849 (bought by 05/23/2023).
The recall record does not specify a remedy, so contact Vital Care Compounder directly for further instructions.
We’ve drafted a message you can send Vital Care Compounder to request your refund or repair — edit it as you like.
Subject: Recall D-0042-2023 — Vital Care Compounder Vital Care Compounder Hello, I own a Vital Care Compounder that is covered by recall D-0042-2023 from Vital Care Compounder. 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.
