FDADecember 7, 2022device

Single-Use Packs, REF: OPO80

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

The hazard

Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or suboptimal vacuum delivered to the phacoemulsification and irrigation/aspiration handpieces during surgery, which could result in surgical delay and/or longer surgical time, which could result in transient corneal edema.

What to do

FDA enforcement status: Ongoing

Brands named

johnson johnson surgical visionjohnsonjohnson johnson

UPCs

05050474573352

Recall history

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

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Single-Use Packs, REF: OPO80 — Recall Details · AllClear