Pharmacy Plus Inc. recalls sterile talc powder vials due to potential contamination from inadequate sterility assurance during production. This affects prescription-only products sold in Hattiesburg, MS. Consumers should contact the manufacturer 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.
Pharmacy Plus Inc. recalls sterile talc powder vials that may not be sterile due to production issues. This poses a risk of infection if used in medical procedures. Affected products were sold in Hattiesburg, Mississippi.
FDA inspections found the products were produced without sufficient sterility assurance. This means the talc powder could contain harmful bacteria or other contaminants that might cause infections when used in medical procedures.
Prescription patients using the recalled sterile talc powder vials for medical purposes. Healthcare providers who dispense the product are at higher risk due to potential contamination.
Check for the product name 'TALC, STERILE POWDER, 5 GM vial' with lot number 65995 and expiration date 10/28/2022. The products were sold by Vital Care Compounder in Hattiesburg, Mississippi.
Look for the lot number 65995 and expiration date 10/28/2022 on the vial.
FDA inspections found the products were produced without sufficient sterility assurance, which could lead to contamination.
The recall record does not specify a remedy, so contact the manufacturer for instructions.
The recall indicates potential contamination, so it is not safe to use without confirming it is not recalled.
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-0055-2023 — Vital Care Compounder Vital Care Compounder Hello, I own a Vital Care Compounder that is covered by recall D-0055-2023 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.
