Imprimis NJOF recalls Dexamethasone Moxifloxacin Ketorolac intraocular injections due to glass particles. Stop using immediately to avoid eye injury.
Presence of particulate matter - Glass like particles.
Imprimis NJOF is recalling Dexamethasone Moxifloxacin Ketorolac intraocular injections because they contain glass particles. Using these injections could cause serious eye injury.
Glass particles in the injection can cause serious eye injury, including damage to the eye tissue or vision loss. This is a safety hazard that requires immediate action.
People who have received this specific eye injection product. Those with eye conditions or recent eye surgery are at higher risk.
Check for the product name Dexamethasone Moxifloxacin Ketorolac, 1 mg/mL, 0.5 mg/mL, or 0.4 mg/mL Single-Use Intraocular Injection. The lot numbers 25APR001A and 25APR001B were produced by Imprimis NJOF, LLC.
Discard the product if you have it. Do not use the injection.
No, the product contains glass particles that can cause serious eye injury. Do not use.
Discard the product immediately and do not use it.
Check for the product name Dexamethasone Moxifloxacin Ketorolac, 1 mg/mL, 0.5 mg/mL, or 0.4 mg/mL Single-Use Intraocular Injection with lot numbers 25APR001A or 25APR001B.
We’ve drafted a message you can send Imprimis NJOF to request your refund or repair — edit it as you like.
Subject: Recall D-0250-2026 — Imprimis NJOF Imprimis NJOF Hello, I own a Imprimis NJOF that is covered by recall D-0250-2026 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.
