ImprimisRx CA, Inc., dba ImprimisRx

FDA Regulatory Profile

ImprimisRx CA, Inc., dba ImprimisRx appears in FDA public data with 4 recalls, 0 510(k) clearances, 1 FDA inspection, and 2 compliance actions on record. Its most recent recall (D-1132-2017, Class II) was initiated on June 23, 2017.

Summary

Total Recalls
4
510(k) Clearances
0
Inspections
1
Compliance Actions
2

Recent Recalls

NumberClassProductDate
D-1132-2017Class IITimolol-Latanoprost PF Solution (0.5-0.005)%, Ophthalmic Drops, Sterile 5ml Bottle, Compounded for aJune 23, 2017
D-1130-2017Class IICurcumin Emulsion 10mg/ml Injection, Sterile 10 mL Multiple Dose Vial, For Slow IV Administration, CJune 23, 2017
D-1131-2017Class IILatanoprost PF Solution, 0.005%, Ophthalmic Drops in Sterile 5ml Bottles, Compounded for a licensed June 23, 2017
D-1133-2017Class IITimolol-Brimonidine-Dorzolamide-Latanoprost (0.5/0.15/2/0.005)% Ophthalmic Drops, Sterile 5ml BottleJune 23, 2017