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Recall Observatory FDA recall evidence

Drug product

Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL, Moxifloxacin 0.6 mg/ 0.6 mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852. NDC 71384-746-06.

D-0251-2026

December 18, 2025

Class II

Product summary

Firm
Imprimis NJOF, LLC
Event
Event 98181
Status
Ongoing
Classification
Class II
Quantity
314 boxes of 6,280 pre-filled syringes
Official record key
drug-enforcement:D-0251-2026

Official wording

Reason: Presence of particulate matter - Glass like particles.

Code information: Lot: 25JAN033A, 25JAN033B, Expires: 02/12/2026.

Distribution pattern: U.S Nationwide

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    particulate matter