FDADecember 3, 2019device

Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14

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

The hazard

Ophthalmic viscosurgical device may be difficult to remove from the eye, leading to increased postoperative intraocular pressure requiring additional intervention. Also, reports of clogging of phacoemulsion equipment tubing, which may lead to delay in the procedure or ocular injury.

What to do

FDA enforcement status: Terminated

Brands named

johnson johnson surgical visionjohnsonjohnson johnson

Recall history

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

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