Vital Care Compounder recalls cyclosporin eye drops due to lack of sterility assurance. Products may be contaminated and cause serious infection. Check lot numbers on packaging for affected items.
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 cyclosporin eye drops that may not be sterile, posing a risk of serious eye infections. Patients using these products should stop using them and contact their doctor.
FDA inspections found the products were made without proper sterility guarantees. This means the eye drops could contain harmful bacteria, leading to infections that might cause vision damage or other serious health issues.
Patients prescribed cyclosporin eye drops by a doctor. Those using the recalled products are at highest risk for serious eye infections.
Check for 10 mL bottles labeled 'CYCLOSPORIN 0.07% OPTH 0.07% Solution' with lot numbers 59638 (bought by 11/25/2022) or 64261 (bought by 04/30/2023).
Immediately stop using the recalled cyclosporin eye drops as they may not be sterile and could cause serious eye infections.
The eye drops may not be sterile, which can lead to serious infections if used.
Look for 10 mL bottles with lot numbers 59638 (bought by 11/25/2022) or 64261 (bought by 04/30/2023).
Yes, if you have the recalled product, stop using it and contact your doctor for alternative treatment.
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-0032-2023 — Vital Care Compounder Vital Care Compounder Hello, I own a Vital Care Compounder that is covered by recall D-0032-2023 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.