Home / Brands / Leica Biosystems Richmond
Leica Biosystems Richmond Recalls
9 recalls on record · June 22, 2016 to September 20, 2017 · Medical Devices
Recalls by year
16
17
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
September 20, 2017Medical DevicesFDA
Leica Biosystems Richmond Inc. recalls Cell Marque, SOX-10 (Polyclonal), 7 mL, REF PA0813, IVD, This antibody is intended for in vitro diagnostic (IVD) use. SO
Hazard: A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.
September 20, 2017Medical DevicesFDA
Leica Biosystems Richmond Inc. recalls Cell Marque, PAX8 (MRQ-50 Mab.), 7 mL, REF PA0808, IVD, This antibody is intended for in vitro diagnostic (IVD) use. PAX
Hazard: A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.
September 20, 2017Medical DevicesFDA
Leica Biosystems Richmond Inc. recalls Cell Marque, Napsin A (MRQ-60 Mab.), 7 mL, REF PA0805, IVD, The antibody is intended for in vitro diagnostic (IVD) use
Hazard: A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.
September 20, 2017Medical DevicesFDA
Leica Biosystems Richmond Inc. recalls Cell Marque, MSH6 (44 Mab.), 7 mL, REF PA0804, IVD, The antibody is intended for in vitro diagnostic (IVD) use. MSH6 i
Hazard: A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.
September 20, 2017Medical DevicesFDA
Leica Biosystems Richmond Inc. recalls Cell Marque, Microphthalmia Transcription Factor (MiTF) (C5/D5 Mab.), 7 mL, REF PA0803, IVD, The antibody is intended
Hazard: A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.
September 20, 2017Medical DevicesFDA
Leica Biosystems Richmond Inc. recalls Cell Marque, Glypican-3 (1G12 Mab), 7 mL, REF PA0800, IVD, The antibody is intended for in vitro diagnostic (IVD) use. G
Hazard: A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.
September 20, 2017Medical DevicesFDA
Leica Biosystems Richmond Inc. recalls Cell Marque, Podoplanin (D2-40 Mab), 7 mL, REF PA0796, IVD, The antibody is intended for in vitro diagnostic (IVD) us
Hazard: A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.
June 29, 2016Medical DevicesFDA
Leica Biosystems Richmond Inc. recalls CytoVision Image Analysis and Capture System, an automated cell-locating device. The Cytovision is a rapid metaphase fin
Hazard: Systems have an improperly activated Windows 7 OS, even though a valid Windows 7 license was associated with each manufactured system. The system appears to be unlicensed. These systems cannot be re-activated using standard Windows licensing procedures and are requiring checks of each potentially affected system to confirm Windows 7 OS is properly activated.
June 22, 2016Medical DevicesFDA
Leica Biosystems Richmond Inc. recalls Ariol is an automated scanning microscope and image analysis system. It is intended for in vitro diagnostic use as an ai
Hazard: An issue during the manufacturing process caused systems to have an improperly activated Windows 7 OS, even though a valid Windows 7 license was associated with each manufactured system.