FDA Device Intelligence
HomeLEICA BIOSYSTEMS NEWCASTLE LTD › BOND™

BOND™

LEICA BIOSYSTEMS NEWCASTLE LTD · Model PA0312 · UDI-DI 05055331304292

MXZ Prescription
10
510(k) clearances
9
Adverse events
3
Recalls
13
Facilities

Description

"BOND Ready-to-Use Primary Antibody Progesterone Receptor (16) is a monoclonal antibody intended to be used for the qualitative identification by light microscopy of human progesterone receptor in formalin-fixed, paraffin-embedded tissue by immunohistochemical staining using the automated BOND-MAX or BOND-III systems."

Recalls

DateFirmReason
2018-08-02Ventana Medical Systems IncLeaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers. A false negative IHC result may occur.
2004-04-06Zymed Laboratories Inc.Mouse anti-TTF-1 had become contaminated by immunoglobulins from mouse serum that was co-eluted during purification leading to false readings.
2004-04-06Zymed Laboratories Inc.Mouse anti-TTF-1 had become contaminated by immunoglobulins from mouse serum that was co-eluted during purification leading to false readings.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.