Pharmacy Plus, Inc. dba Vital Care Compounder recalls 10mL droptainers for PRED ACETATE/GATIFLOXACIN 1%/0.5% suspensions due to lack of sterility assurance found in FDA inspections. Products may cause infections if used without proper sterility.
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 specific 10mL droptainers for PRED ACETATE and GATIFLOXACIN medications because FDA inspections found they cannot guarantee sterility. Using these products could lead to infections if not properly sterilized.
FDA inspections found the droptainers were produced without proper sterility assurance. This means the products may not be sterile when used, potentially causing infections if injected or administered improperly.
Prescription medication users who received these specific droptainers from the manufacturer. Patients using the recalled products for medical treatment are at risk of infection.
Check for the product name 'PRED ACETATE / GATIFLOXACIN 1% / 0.5% SUSP, 10 mL droptainers' and lot numbers 65056 (BUD: 11/18/2022) or 66246 (BUD: 11/19/2022).
Identify the lot number and expiration date on the droptainer to confirm if it's part of the recall.
FDA inspections found the droptainers were produced without proper sterility assurance, which could lead to infections if used improperly.
The recall record does not specify a remedy, so contact the manufacturer for guidance.
Yes, lot numbers 65056 (BUD: 11/18/2022) and 66246 (BUD: 11/19/2022) are part of this recall.
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-0051-2023 — Vital Care Compounder Vital Care Compounder Hello, I own a Vital Care Compounder that is covered by recall D-0051-2023 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.
