FDAMay 15, 2023device

OEC 9900 Systems with 9-inch Image Intensifier

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

The hazard

Image intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, hematoma, contusion, bruise, pain.

What to do

FDA enforcement status: Ongoing

Brands named

ge oec medical systems

UPCs

00840682114301

Recall history

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

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OEC 9900 Systems with 9-inch Image Intensifier — Recall Details · AllClear