Imprimis NJOF, LLC recalled 778 boxes of Dexamethasone Moxifloxacin intraocular injection on December 18, 2025. The recall stems from the presence of glass-like particles in the product. Consumers and healthcare providers should stop using the product immediately.
Presence of particulate matter - Glass like particles.
Consumers and healthcare providers should stop using this product immediately. Contact Imprimis NJOF, LLC or your healthcare provider for guidance. Notification method: Letter
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Dexamethasone Moxifloxacin is an intraocular injection used primarily in eye surgeries or treatments to prevent infection and reduce inflammation. Consumers typically purchase this product through healthcare providers for specific medical conditions.
The presence of glass-like particles can lead to serious complications if injected into the eye, potentially causing injury to the eye or surrounding tissues. This hazard is significant due to the sensitive nature of intraocular applications.
This recall is not part of a broader industry pattern.
Consumers face a significant safety risk if they have this product. Immediate action is necessary to prevent potential health complications.
Lot numbers and expiration dates can typically be found on the packaging or the syringe label.
Expect a refund processing timeline of approximately 4-6 weeks after returning the product.
Keep records of your purchase, including receipts and any correspondence regarding the recall.
The recalled product is Dexamethasone Moxifloxacin, available in 1 mg/mL and 5 mg/mL concentrations, packaged in 1 mL pre-filled syringes. The lot numbers affected include 25MAY051 and 25AUG003, with expiration dates of June 26, 2026, and August 7, 2026, respectively.
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