Leica Microsystems, Inc. recalls

31 recalls on record · latest: November 21, 2022

Official U.S. recall history for Leica Microsystems, Inc., compiled from official government records.

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Leica MICROSYSTEMS M530 OHX recalled over fire hazard

November 21, 2022 · Medical device recalls Moderate risk There is a potential issue resulting in the Power Supply potentially becoming o…

Leica MICROSYSTEMS Provido recalled over fire hazard

November 21, 2022 · Medical device recalls Moderate risk There is a potential issue resulting in the Power Supply potentially becoming o…

Leica MICROSYSTEMS Proveo 8 recalled over fire hazard

November 21, 2022 · Medical device recalls Moderate risk There is a potential issue resulting in the Power Supply potentially becoming o…

Leica Microsystems, Inc. recalls Leica Surgical Operating Microscopes, M530 OHX, Part Number 10448737

August 26, 2022 · Medical device recalls Moderate risk During internal testing, Leica Microsystems has become aware of a component cha…

Leica Microsystems, Inc. recalls Leica Surgical Operating Microscopes, ARveo 8, Part Number 10449063

August 26, 2022 · Medical device recalls Moderate risk During internal testing, Leica Microsystems has become aware of a component cha…

Leica Microsystems, Inc. recalls Leica Surgical Operating Microscopes, Arveo, Part Number 10448999

August 26, 2022 · Medical device recalls Moderate risk During internal testing, Leica Microsystems has become aware of a component cha…

Leica Microsystems, Inc. recalls Leica Surgical Operating Microscopes, PROvido Part Numbers: a. 10448976, b. 10448950

August 26, 2022 · Medical device recalls Moderate risk During internal testing, Leica Microsystems has become aware of a component cha…

Leica Microsystems, Inc. recalls Leica Microsystems M220 F12 Microscope Systems

November 3, 2021 · Medical device recalls Moderate risk In May 2021, Leica Microsystems received one (1) complaint pertaining to the M2…

Leica Microsystems, Inc. recalls BOND Ready-To-Use Primary Antibody CDX2 (EP25), REF PA0375

July 30, 2021 · Medical device recalls Moderate risk Product may not perform as specified in IFU.

Leica Microsystems, Inc. recalls Leica ARveo and M530 OH6 microscope systems.

May 20, 2020 · Medical device recalls Moderate risk Possible unintended interruption of surgical procedures due to equipment shutdo…

Leica Microsystems, Inc. recalls BOND Polymer Refine Detection Kit, Catalog No. DS9800. This detection system is for in vitro diagnostic use. Bond Polym…

November 18, 2019 · Medical device recalls Moderate risk BOND Polymer Refine Detection kits (DS9800) were held out of refrigerated stora…

Leica Microsystems, Inc. recalls Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…

May 3, 2019 · Medical device recalls Moderate risk The current labelling does not include any specific warning about usage of flam…

Leica Microsystems, Inc. recalls Leica M220 F12 surgical microscope The Leica M220 F12 surgical microscope is an optical instrument for improving the vi…

January 2, 2019 · Medical device recalls Moderate risk The M220 optics may unintentionally drop into the surgical field, risking conta…

BOND Slide Labeler Zebra Printer and recalled over fire hazard

September 17, 2018 · Medical device recalls Moderate risk The power supply unit for the printer used with the device can potentially over…

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

September 4, 2018 · Medical device recalls Moderate risk The firm received complaints that the instrument tipped over when the swing arm…

Leica Microsystems, Inc. recalls Leica HistoCore SPECTRA CV Coverslipper, used in preparation of histological and cytological tissue samples for microsc…

September 4, 2018 · Medical device recalls Moderate risk Product was assembled with an isolating fiberglass hose within the oven in the…

Leica Microsystems, Inc. recalls Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.

June 25, 2018 · Medical device recalls Moderate risk Recall is due to a design weakness of the power insert module.

Leica Microsystems, Inc. recalls Leica Biosystems HistoCore SPECTRA ST, Slide Stainer, Automated Product Usage: The intended use of this device is a sta…

June 13, 2018 · Medical device recalls Moderate risk These devices have an incorrect specification against safety standard ISO61010-…

Leica Microsystems, Inc. recalls Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419, 1044…

June 4, 2018 · Medical device recalls Moderate risk Possible failure of screws which hold the gas spring fixation bracket in place.…

Leica Microsystems, Inc. recalls PROVEO 8 Ophthalmic Microscope System optical instrument for improving the visibility of objects through magnification…

September 25, 2017 · Medical device recalls Moderate risk The observed issues can lead to unexpected interruptions of the optics carrier…

Nussloch GmbH ASP6025 Tissue Processor recalled over labeling errors

June 19, 2017 · Medical device recalls Moderate risk Incorrect labeling for specified voltage for the Alarm Connectors on the rear s…

Leica Microsystems, Inc. recalls Novocastr Liquid Mouse Monoclonal Antibody CDX2 (CDX2) is recommended for the assessment of CDX2 protein in normal and…

April 5, 2016 · Medical device recalls Moderate risk Testing of retained units indicated that Lot numbers of CDX2 indicated are not…

Leica Microsystems, Inc. recalls Novocastr Liquid Mouse Monoclonal Antibody Renal Cell Carcinoma Marker (RCC) is recommended for use as part of a panel…

April 5, 2016 · Medical device recalls Moderate risk Testing of retained units indicated that Lot numbers of CDX2 and RCC indicated…

Leica Microsystems, Inc. recalls Novocastra Liquid Mouse Monoclonal Antibody Calretinin, NCL-L-CALRET-566. Intended for the qualitative identification b…

March 22, 2016 · Medical device recalls Moderate risk Novocastra Liquid Mouse Monoclonal Antibody Calretinin when used in combination…

Leica Microsystems Ag recalled over fire hazard

January 11, 2016 · Medical device recalls Moderate risk An electronic component of the Leica M525 OH4 and Leica M720 OH5 surgical micro…

Leica Microsystems, Inc. recalls This reagent is for in vitro diagnostic use. Pax-5 (1EW) monoclonal antibody is intended to be used for the qualitative…

December 30, 2015 · Medical device recalls Moderate risk The Bond" Polymer Refine Detection and Novolink" Polymer Detection System may n…

Leica Microsystems, Inc. recalls Bond Polymer Refine Red Detection DS9390 kits. The common name of the device is detection system for in vitro diagnosti…

November 27, 2015 · Medical device recalls Moderate risk The Firm informed the importer/distributor, Leica Microsystems, a manufacturing…

Leica Microsystems, Inc. recalls Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10). Immunohistochemistry. in vitro diagnostic. 0.1ml NCL-CD10…

September 3, 2015 · Medical device recalls Moderate risk These Lot numbers are not stable up to the expiry date on the product labeling.

Leica Microsystems, Inc. recalls The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology Departments. The Leica ASP200S/ASP300S Tissue Proc…

August 5, 2015 · Medical device recalls The Leica ASP200S/ASP300S Tissue Processor have an incorrect internal wiring to…

Leica Microsystems, Inc. recalls The Leica ASP6025 Tissue Processor. Pathology and Hematology Departments. The Leica ASP6025 Tissue Processor is an auto…

July 27, 2015 · Medical device recalls Moderate risk The ASP6025 Tissue Processor instrument is incorrectly getting into a state of…

Leica Microsystems, Inc. recalls Liquid Mouse Monoclonal Antibody CD15 used is laboratories to perform immunohistochemical (IHC) staining. Product Usage…

December 16, 2014 · Medical device recalls Moderate risk The staining intensity decreases over the shelf life.