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FDADecember 20, 2018drug

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

GMP Deviations: A silicone particulate was noted in Ozurdex.

What to do

FDA enforcement status: Completed

Brands named

allergan plcallerganallergan plc

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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