Dexamethasone Moxifloxacin Ketorolac recall: Particulate Matter
Dexamethasone Moxifloxacin Ketorolac, 1 mg/mL, 0.5 mg/mL, 0.4 mg/mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit…
Why was Dexamethasone Moxifloxacin Ketorolac recalled?
Presence of particulate matter - Glass like particles.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot: 25APR001A, 25APR001B, Expires: 04/03/2026.
- Product
- Dexamethasone Moxifloxacin Ketorolac, 1 mg/mL, 0.5 mg/mL, 0.4 mg/mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit…
- Recalling firm
- Imprimis NJOF, LLC
- Quantity
- 596 boxes of 11,920 pre-filled syringes
- Distribution
- U.S Nationwide
- Recall date
- January 14, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (drug)