FDAFDA · Food and drugs·Recall number D-0251-2026
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.
Published January 14, 2026 · Recall initiated: December 18, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of particulate matter - Glass like particles.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Imprimis NJOF, LLC
- Distributor
- U.S Nationwide
- Lot
- Lot: 25JAN033A, 25JAN033B, Expires: 02/12/2026.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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