Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac recall: Subpotent
Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic Solution 1%, 0.5%, 0.075%, 8mL, Compounded By: Imprimis NJOF, LLC. 1705 Route…
Why was Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac recalled?
Subpotent Drug
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 #: 23JUN031; Exp. 07/03/2024
- Product
- Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic Solution 1%, 0.5%, 0.075%, 8mL, Compounded By: Imprimis NJOF, LLC. 1705 Route…
- Recalling firm
- Imprimis NJOF, LLC
- Quantity
- 3320 bottles
- Distribution
- U.S. Nationwide
- Recall date
- May 8, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (drug)