Z-1726-2014 Class II Terminated

Recalled by Leica Microsystems, Inc. — Buffalo Grove, IL

FDA device recall Z-1726-2014 was initiated by Leica Microsystems, Inc. on Sep 11, 2013 and is designated Class II. Reason for recall: 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… The recall status is terminated (terminated Apr 24, 2017). Affected quantity: 103 total.

Recall Details

Product Type
Devices
Report Date
Jun 18, 2014
Initiation Date
Sep 11, 2013
Termination Date
Apr 24, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
103 total

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.

Reason for Recall

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 Pattern

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.

Code Information

Leica Ceiling Mounts MS-1F, MC-1F; Article Numbers: 10446657, 10446658

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-1726-2014
openFDA file date
Oct 27, 2026
Loaded by RegDataLab
Oct 29, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.