FDAAugust 2, 2024device

Monarch Platform (Urology), REF: MON-000007, MON-000007-RFB

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

The hazard

Endoscopy/bronchoscopy/urology devices may have a strain relief defect with some cart and tower power cords that may cause an electrical short, which may lead to system shutdown, which can lead to prolonged procedure or case conversion, and if the user (e.g., operating room staff) touches exposed wires or conductive fluids in contact with the exposed wires, there is a chance of electrical shock.

What to do

FDA enforcement status: Ongoing

Brands named

auris healthauris

UPCs

304003613003040036070010810068810889

Recall history

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

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