Prednisolone-Moxifloxacin-Bromfenac Sterile Ophthalmic recall: Sterility Concern
Prednisolone-Moxifloxacin-Bromfenac Sterile Ophthalmic Suspension, 1%, 0.5%, 0.075%, 5mL, Quantity: 20mL, Rx Only, Compounded by: Imprimis NJOF, LLC.…
Why was Prednisolone-Moxifloxacin-Bromfenac Sterile Ophthalmic recalled?
Lack of Assurance of Sterility
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: 23NOV018 Exp. 6/17/24
- Product
- Prednisolone-Moxifloxacin-Bromfenac Sterile Ophthalmic Suspension, 1%, 0.5%, 0.075%, 5mL, Quantity: 20mL, Rx Only, Compounded by: Imprimis NJOF, LLC.…
- Recalling firm
- Imprimis NJOF, LLC
- Quantity
- 4,280 boxes
- Distribution
- US Nationwide
- Recall date
- June 19, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (drug)