FDA recall record

Leica Ceiling Mount MS-1F & MC-1F for use with the M500 N operating microscope recall — FDA Z-1726-2014

The ceiling mount supplier encountered an event in which the drive screw in the motor unit, which lifts and lowers the lower lift arm, broke. As a result,…

Class IIclassification
Z-1726-2014official record ID
Jun 18, 2014report date

Recall record at a glance

Official recordZ-1726-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLeica Microsystems, Inc.
Report dateJun 18, 2014
Recall initiation dateSep 11, 2013
Quantity103 total
LocationBuffalo Grove, IL, United States

Official product description

Leica Ceiling Mount MS-1F & MC-1F for use with the M500 N operating microscope. Article Number 10446657 utilizes a supply voltage of 110 V. Article Number 10446658 utilizes a supply voltage of 220 V. Intended to be used for improving the visibility of objects through magnification and illumination.

Why the product was recalled

The ceiling mount supplier encountered an event in which the drive screw in the motor unit, which lifts and lowers the lower lift arm, broke. As a result, the lift arm fell down approx. 60 cm (23.6 inches).

Distribution information

Worldwide Distribution -- USA, including the states of AZ, IL, MA, MO, NC, OR, TX, VA, and WI; and, the countries of Australia, Austria, Chile, China, Colombia, Czech Republic, Greece, Israel, Italy, Japan, Malaysia, Netherlands, Norway, Oman, Saudi Arabia, South Korea, Spain, Sweden, Switzerland, and United Kingdom.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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