Imprimis recalls Dexamethasone Moxifloxacin eye injections due to glass particles. These injections are for prescription use only and may cause injury if particles enter the eye.
Presence of particulate matter - Glass like particles.
Imprimis is recalling Dexamethasone Moxifloxacin eye injections (1 mg/mL and 5 mg/mL) because they contain glass-like particles. This could cause eye injury if the particles enter the eye during use.
Glass-like particles in the injection could enter the eye during administration, potentially causing injury. This is a serious hazard for patients receiving the medication.
Prescription patients using this eye injection for medical treatment. People with eye conditions requiring this medication are most at risk.
Check for the product name 'Dexamethasone Moxifloxacin', strength 1 mg/mL or 5 mg/mL, 1 mL, and the lot numbers 25MAY051 or 25AUG003. The product is sold by Imprimis NJOF, LLC in New Jersey.
Look for the lot numbers 25MAY051 or 25AUG003 on the packaging.
The recall states the product contains glass-like particles, which could cause eye injury. Do not use until the recall is resolved.
Check for the lot numbers 25MAY051 or 25AUG003 on the packaging. The product is sold by Imprimis NJOF, LLC in New Jersey.
The recall does not specify a remedy, so contact your doctor or pharmacist for guidance.
We’ve drafted a message you can send Imprimis to request your refund or repair — edit it as you like.
Subject: Recall D-0249-2026 — Imprimis Imprimis Hello, I own a Imprimis that is covered by recall D-0249-2026 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.
