Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Dexamethasone Moxifloxacin 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, 1 mg/mL and 5 mg/mL, 1 mL Intraocular Injection, Rx only, Imprimis NJOF, LLC, Ledgewood, NJ 07852, NDC 71384-512-0.1
Quantity: 778 boxes of 15,540 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