ORTHO VISION recall in Canada: Software anomaly
This recall involves ORTHO VISION and ORTHO VISION Max Analyzers sold in Canada. They are being recalled due to a softwa...
Medical device recalls in Canada cover implants, surgical equipment, and diagnostic tools. These recalls are issued by Health Canada.
4,400 recalls found
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This recall involves ORTHO VISION and ORTHO VISION Max Analyzers sold in Canada. They are being recalled due to a softwa...
This recall involves the Lithium Assay System and Alinity c Lithium Reagent Kit sold in Canada. It's being recalled beca...
This recall involves non-absorbable synthetic surgical mesh for pelvic organ prolapse (POP) repair sold in Canada. It's
This recall involves Basis Alginate 6 lb and 25 lb Cinnamon products sold in Canada. It's being recalled because metal s...
This recall involves Alpha Conducting Solution sold in Canada. It's being recalled because the solution failed antimicro...
This recall involves the Monaco RTP System, a medical device used in Canada. It's being recalled because monitor units c...
This recall involves Merge PACS and Merge ORTHOPACS software versions 7.3, 7.3.1, 8.0, and 8.0.1. It's being recalled be...
This recall involves the Cartilage MICROTOME and Cartilage MICROTOME Handle sold in Canada. It's being recalled because
This recall involves Brilliance and Ingenuity CT Systems sold in Canada. They are being recalled because images may be i...
This recall involves the ABL90 FLEX - Analyzer, a medical device used in Canada. It's being recalled because a software
This recall involves Oragene DNA collection devices sold in Canada. It's being recalled because the ink on the label may...
This recall involves the Volumat MC Agilia CA volumetric infusion pump sold in Canada. It's being recalled because of so...
This recall involves MED-RX Hydrophobic Insufflation Filters sold in Canada. They are being recalled because the filter
This recall involves the Elekta UNITY medical device sold in Canada. It's being recalled because incorrect software sett...
This recall involves Azurion 7 M12 and M20 medical devices sold in Canada. It's being recalled because the system may ta...
This recall involves Azurion 7 M12 and M20 medical devices sold in Canada. They are being recalled because the automatic...
This recall involves Tina-Quant Myoglobin Gen.2, a medical device used for testing. It's being recalled because of quali...
This recall involves the MOBILETT Elara Max medical device sold in Canada. It's being recalled because a firmware issue
This recall involves a reported shortage of EpiPen (0.3 mg) auto-injectors in Canada. Pfizer Canada is managing distribu...
This recall involves AQUIOS IMMUNO-TROL Low Cells sold in Canada. It's being recalled because it may cause inaccurate te...
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