Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Dexamethasone Moxifloxacin Ketorolac Recalled by Imprimis NJOF, LLC Due to Presence of particulate matter - Glass like particles.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Imprimis NJOF, LLC directly.
Affected Products
Dexamethasone Moxifloxacin Ketorolac, 1 mg/mL, 0.5 mg/mL, 0.4 mg/mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-513-01.
Quantity: 596 boxes of 11,920 pre-filled syringes
Why Was This Recalled?
Presence of particulate matter - Glass like particles.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Imprimis NJOF, LLC
Imprimis NJOF, LLC has 21 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report