FDAApril 26, 2024device

O-arm O2 Imaging System-Mobile x-ray system designed for 2D fluoroscopic and 3D imaging for adult and pediatric patients. Product Number: BI70002000

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

The hazard

Potential for an electrical component of the O-arm" O2 Imaging System to intermittently shut off,failure can cause the potential for surgical delay, additional imaging, cancellation and rescheduling of surgery, or completion of surgery without the benefit of image guidance.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic navigation inc littletonmedtronicmedtronic navigation

Recall history

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

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