Imprimis NJOF recalls specific lots of moxifloxacin eye injection vials due to lack of sterility assurance. This could lead to infections if used improperly. Check your NDC and expiration dates.
Lack of Assurance of Sterility
Imprimis NJOF has recalled certain lots of moxifloxacin 4 mg/0.8 mL vials for eye injections because they may not be sterile. Using these vials could lead to serious eye infections if they become contaminated.
The vials lack assurance of sterility, meaning they could be contaminated with bacteria. If used for eye injections, this contamination could cause serious eye infections or other complications.
Prescription eye drop users who have the recalled vial lots. Patients receiving eye injections from this product are at risk of infection.
Check the NDC number 71384-511-08 and expiration dates listed in the recall notice. The specific lots include 23JUN003 through 24FEB027 with varying expiration dates.
Look for the lot number on the vial label, which is listed in the recall as 23JUN003 through 24FEB027.
The product was recalled due to a lack of assurance of sterility, which could lead to contamination and serious eye infections if used.
Check the vial lot number and expiration date. If it matches the recalled lots, stop using it and contact your healthcare provider.
Yes, using contaminated vials could cause serious eye infections. The recall is for safety reasons.
We’ve drafted a message you can send Imprimis NJOF to request your refund or repair — edit it as you like.
Subject: Recall D-0516-2024 — Imprimis NJOF Imprimis NJOF Hello, I own a Imprimis NJOF that is covered by recall D-0516-2024 from Imprimis NJOF. 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.
