FDAJune 9, 2009device

NDI P7 Position Sensor, Stereotaxic Instrument

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

The hazard

Zimmer CAS voluntarily conducted a retrospective recall on specific P7 Position Sensors (Cameras), installed on Sesamoid and Sesamoid Plasty CAS workstations due to a series of these components determined to be affected with a manufacturing issue whereby they may potentially stop functioning during usage.

What to do

FDA enforcement status: Terminated

Brands named

orthosoft inc dba zimmer casorthosoftorthosoft inc

Recall history

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

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