FDANovember 3, 2021device

Leica Microsystems M220 F12 Microscope Systems

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

The hazard

In May 2021, Leica Microsystems received one (1) complaint pertaining to the M220 F12 Surgical Microscope system. There was no patient injury reported for this complaint. However, the identified defect carries some potential injury risk. In the event that this defect may occur, the M220 optics carrier may unintentionally drop into the surgical field, risking contact with the patient.

What to do

FDA enforcement status: Terminated

Brands named

leica microsystemsleica

UPCs

07630003552188

Recall history

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

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