Imprimis NJOF recalls prednisolone-moxifloxacin-bromfenac sterile eye drops (1%, 0.5%, 0.075%) with risk of contamination. Product was compounded by Imprimis NJOF, LLC in New Jersey. No remedy specified in recall notice.
Lack of Assurance of Sterility
Imprimis NJOF has recalled prednisolone-moxifloxacin-bromfenac sterile eye drops that may not be sterile. This could lead to eye infections if used. The recall covers specific lot numbers and expiration dates.
The product lacks assurance of sterility, meaning it could contain harmful bacteria or other contaminants. Using contaminated eye drops might cause serious eye infections, especially for individuals with compromised immune systems or existing eye conditions.
Prescription eye drop users who received this specific compounded product from Imprimis NJOF, LLC in New Jersey. People with eye conditions requiring these medications are most at risk.
Check for the product name 'Prednisolone-Moxifloxacin-Bromfenac Sterile Ophthalmic Suspension' with the lot number 23NOV018 and expiration date 6/17/24. The product was compounded by Imprimis NJOF, LLC in New Jersey.
Look for the lot number 23NOV018 and expiration date 6/17/24 on the product label.
The recall states there is a lack of assurance of sterility, so the product may not be safe. Do not use it until the recall is resolved.
Check for the lot number 23NOV018 and expiration date 6/17/24 on the product label. The product was compounded by Imprimis NJOF, LLC in New Jersey.
The recall notice does not specify a remedy, so contact the manufacturer directly for guidance.
We’ve drafted a message you can send Imprimis NJOF to request your refund or repair — edit it as you like.
Subject: Recall D-0548-2024 — Imprimis NJOF Imprimis NJOF Hello, I own a Imprimis NJOF that is covered by recall D-0548-2024 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.
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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.
