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BOND™

LEICA BIOSYSTEMS NEWCASTLE LTD · Model PA0435 · UDI-DI 05055331304100

NJT Prescription

510(k) clearances

Adverse events (1 deaths)

Recalls

Facilities

Description

Neuron Specific Enolase (22C9) monoclonal antibody is intended to be used for the qualitative identification by light microscopy of human neuron specific enolase in formalin-fixed, paraffin-embedded tissue by immunohistochemical staining using the automated BOND system (includes Leica BOND-MAX system and Leica BOND-III system).

Recalls

Date	Firm	Reason
2025-11-03	GET TESTED INTERNATIONAL AB	Distribution without premarket approval/clearance.
2025-08-11	Agilent Technologies Denmark ApS	Their is the potential for weak staining which may result in false negative CD20 identification.
2025-08-11	Agilent Technologies Denmark ApS	Their is the potential for weak staining which may result in false negative CD20 identification.
2025-08-11	Agilent Technologies Denmark ApS	Their is the potential for weak staining which may result in false negative CD20 identification.
2024-06-27	Ventana Medical Systems, Inc.	Their is a potential for high background and off-target staining when using the monoclonal primary antibody which can result in false positive results.
2021-07-30	Leica Microsystems, Inc.	Product may not perform as specified in IFU.
2021-07-15	Cell Marque Corporation	Mouse Monoclonal Antibody labelled with an incorrect expiry date of 31 Dec 2023. The correct expiry date is 31 Dec 2022. If used beyond expiry, the material performance is likely t
2019-11-18	Leica Microsystems, Inc.	BOND Polymer Refine Detection kits (DS9800) were held out of refrigerated storage longer than specified which may exhibit suboptimal staining.
2019-10-10	Biocare Medical, LLC	Firm has identified product has no staining. If used, may result in invalid test results when used with controls in the clinical setting. Positive control would observe no staining
2018-08-02	Ventana Medical Systems Inc	Leaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers. A false negative IHC result may occur.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.