Imprimis recalls specific lots of Dexamethasone-Moxifloxacin eye injection vials due to lack of sterility assurance. These vials are for intraocular use only and may cause infection if used.
Lack of Assurance of Sterility
Imprimis is recalling certain lots of Dexamethasone-Moxifloxacin eye injection vials because they lack sterility assurance. Using these vials could lead to eye infections if they are not properly sterile.
The vials may not be sterile, which could lead to eye infections if used for intraocular injections. This is a risk for patients who have been prescribed this medication by a healthcare provider.
Patients prescribed this medication by a doctor for eye injections. Those with the specific lot numbers listed in the recall are most at risk.
Check the lot number on the vial label: 23MAY016, 23JUL016, 23AUG034, or 23DEC014. These vials are for intraocular injection only and were manufactured by Imprimis NJOF, LLC.
Look for lot numbers 23MAY016, 23JUL016, 23AUG034, or 23DEC014 on the vial label.
No, these vials lack sterility assurance and could cause eye infections if used for intraocular injections.
Check the lot number on the vial label. If it matches the recalled lots, contact your doctor or pharmacist for guidance.
The vials have specific lot numbers: 23MAY016, 23JUL016, 23AUG034, or 23DEC014. They are for intraocular injection only.
We’ve drafted a message you can send Imprimis to request your refund or repair — edit it as you like.
Subject: Recall D-0513-2024 — Imprimis Imprimis Hello, I own a Imprimis that is covered by recall D-0513-2024 from Imprimis. 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.
