Tri-Moxi+¿
Presence of particulate matter - Glass like particles.
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Subpotent Drug
Cause type: Wrong potency / content
Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.
Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic Solution 1%, 0.5%, 0.075%, 8mL, Compounded By: Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B Ledgewood, NJ 07852, NDC 71384-340-08
Compare with the code on your package — it is the most precise check available.
Drug: Moxifloxacin Category: Eye Drops & Ophthalmic
Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.
Presence of particulate matter - Glass like particles.
Presence of particulate matter - Glass like particles.
Presence of particulate matter - Glass like particles.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Presence of particulate matter - Glass like particles.
Presence of particulate matter - Glass like particles.
Presence of particulate matter - Glass like particles.
Subpotent Drug
Free recall alerts
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.