PlainRecalls
FDA Drug Low Class III Ongoing

Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-733-05.

Reported: July 30, 2025 Initiated: July 9, 2025 #D-0536-2025

Product Description

Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-733-05.

Reason for Recall

Sub-Potent Drug: Subpotent assay results during stability testing.

Details

Recalling Firm
Imprimis NJOF, LLC
Units Affected
2,890 vials
Distribution
Nationwide in the USA
Location
Ledgewood, NJ

Frequently Asked Questions

What product was recalled?
Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-733-05.. Recalled by Imprimis NJOF, LLC. Units affected: 2,890 vials.
Why was this product recalled?
Sub-Potent Drug: Subpotent assay results during stability testing.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 30, 2025. Severity: Low. Recall number: D-0536-2025.