OZURDEX (dexamethasone intravitreal implant) 0.7 mg), 1 single-use plastic applicator contained within carton, Rx only, Allergan Inc Irvine, CA 92612, NDC 0023-3348-07
Recall Number: D-0387-2019
Firm: Allergan, PLC.
Classification: Class II
Status: Completed
Report Date: 20190116
Initiation Date: 20181220
Termination Date:
Reason for Recall
GMP Deviations: A silicone particulate was noted in Ozurdex.
Product Description
OZURDEX (dexamethasone intravitreal implant) 0.7 mg), 1 single-use plastic applicator contained within carton, Rx only, Allergan Inc Irvine, CA 92612, NDC 0023-3348-07