Medical device recalls Moderate risk

Leica Microsystems, Inc. recalls Leica M525 F20 Surgical Microscope System

Recall date
September 4, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-3175-2018
FDA classification
Class II
Brand / firm
Leica Microsystems, Inc.
Sold / distributed
US and Canada

Why it was recalled

The firm received complaints that the instrument tipped over when the swing arm was fully extended.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Leica M525 F20 Surgical Microscope System

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