Leica Microsystems, Inc.: Medical Device Recalls in 2018

According to to data from the FDA, there were 6 medical device recalls made by Leica Microsystems, Inc. in 2018. See the details of the recalls below.

You can see similar recalls for other firms.

• Leica Biosystems HistoCore SPECTRA ST, Slide Stainer, Automated Product Usage: The intended use of this device is a stainer for laboratory applications and intended for the preparation of histological and cytological specimens.
• Leica HistoCore SPECTRA CV Coverslipper, used in preparation of histological and cytological tissue samples for microscopic analysis for medical diagnostics.
• BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301, for use with BOND-III and BOND-MAX instruments
• Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419, 10448420, 10448485, 10448486 Product Usage: Intended use of this device is an optical instrument for magnifying and illuminating specimens. It can be applied for observation and documentation and for human and veterinary medical treatment. Not for use in Eye Operations.
• Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.
• Leica M525 F20 Surgical Microscope System