Imprimis NJOF Recalls

3 recalls found for Imprimis NJOF. Check if any of your products are affected.

HIGHFDA DRUG

Imprimis NJOF Recalls Intraocular Injection Over Glass Particles

Imprimis NJOF, LLC recalled 314 boxes of Tri-Moxi+¿ intraocular injections on December 18, 2025. The recall is due to the presence of glass-like particles in the product. Consumers and healthcare providers should stop using the product immediately and contact the company for further guidance.

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HIGHFDA DRUG

Imprimis NJOF Recalls Intraocular Injection Due to Glass Particles

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.

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Brand Statistics

Total Recalls
3
Pages
1