FDAApril 3, 2020device

ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as pre-operative software for simulating and evaluating surgical treatment options

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

The hazard

Observed an internal repetitive software glitch in ImmersiveView.

What to do

FDA enforcement status: Ongoing

Brands named

immersivetouch

Recall history

No related federal recalls on record for this brand yet.

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ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as pre-operative software for simulating and evaluating surgical treatment options — Recall Details · AllClear