FDAOctober 5, 2016device

Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm (EMS) The system is intended for use in surgical operating rooms (OR) or intraoperative surgical/imaging rooms where simultaneous multiple image viewing is required

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

The hazard

The Drager Pendula spring arm device has a set of screws located on the spring arm that were not properly secured with Loctite and may become loose.

What to do

FDA enforcement status: Terminated

Brands named

steris

Recall history

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

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