Pharmacy Plus, Inc. dba Vital Care Compounder recalls sterile injectable drug solutions that may not be sterile, posing a risk of infection. Affected products include specific vials with lot numbers 66369 and 66540.
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 sterile injectable drug solutions that may not be sterile. This could lead to infections if used improperly. The recall affects specific vials with lot numbers 66369 and 66540.
The FDA found that the products were produced without sufficient assurance of sterility. This means the solutions could contain harmful bacteria, leading to infections if injected.
Prescription drug users who received the recalled vials with lot numbers 66369 (BUD: 11/06/2022) or 66540 (BUD: 11/09/2022) from Vital Care Compounder. Healthcare providers and patients using these products are at risk.
Check for vials labeled 'PAP/PHEN/PROSTAG/ATROPINE INJ 150MG/7.5MG/75MCG/1MG' with lot numbers 66369 or 66540. These were sold by Vital Care Compounder in Mississippi.
Look for lot numbers 66369 or 66540 on the vial label.
The FDA found that the products were produced without sufficient assurance of sterility, which could lead to infections if used.
The recall does not specify a remedy, so check the lot number and contact Vital Care Compounder for further instructions.
Yes, the products may not be sterile, which could cause infections if injected.
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-0041-2023 — Vital Care Compounder Vital Care Compounder Hello, I own a Vital Care Compounder that is covered by recall D-0041-2023 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.
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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.
