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Cellavision AB Recalls
2 recalls on record · June 20, 2018 to November 26, 2025 · Medical Devices
Recalls by year
18
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 26, 2025Medical DevicesFDA
Cellavision AB recalls REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60, IVD in conjunction with a Honeywell Vuquest
Hazard: Automated cell-locating device barcode reader may read the barcode of the previously processed slide resulting in a misattribution of diagnostic results.
June 20, 2018Medical DevicesFDA
Cellavision AB recalls CellaVision DM Software versions 6.0.1 or 6.0.2 installed on the following products: CellaVision DM96, DM1200, DM9600 an
Hazard: A software malfunction was found where WBC, RBC and PLT comments added after a slide is signed, are not sent to the LIS. This can only occur where customers process multiple slides per blood sample.