Pharmacy Plus Inc. recalls Brilliant Blue G 0.04% Solution vials (Rx only) produced without sterility assurance. FDA inspection found these products may not be sterile, posing infection risks. 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 Brilliant Blue G 0.04% Solution vials (2 mL, Rx only) because FDA found they were produced without sterility assurance. Using these vials could lead to infections if the solution isn't sterile.
FDA inspections found the vials were produced without sterility assurance. This means the solution might not be sterile, which could cause infections if used in medical treatments.
Prescription drug users who received the recalled vials from pharmacies or healthcare providers. Patients using these vials for medical treatments are at risk of infection.
Check for vials labeled 'BRILLIANT BLUE G, 0.04% Solution, 2 mL' with lot number 60448, produced by Vital Care Compounder. These vials were sold starting October 31, 2022.
Reach out to Pharmacy Plus Inc. at 115 S. 40th Ave., Hattiesburg, MS 39402 for details on the recall and next steps.
FDA inspections found the vials were produced without sterility assurance, meaning they might not be sterile and could cause infections.
Contact Pharmacy Plus Inc. at 115 S. 40th Ave., Hattiesburg, MS 39402 for details on the recall and next steps.
Yes, the recalled vials have lot number 60448, produced on October 31, 2022.
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-0029-2023 — Vital Care Compounder Vital Care Compounder Hello, I own a Vital Care Compounder that is covered by recall D-0029-2023 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.
