Biograph mMR System recall in Canada: Suboptimal PET motion correction
This recall involves the Biograph mMR System sold in Canada. It's being recalled because the BodyCOMPASS functionality f...
Medical device recalls in Canada cover implants, surgical equipment, and diagnostic tools. These recalls are issued by Health Canada.
4,400 recalls found
Page 190 of 220
This recall involves the Biograph mMR System sold in Canada. It's being recalled because the BodyCOMPASS functionality f...
This recall involves Hemoglobin A1c Controls Level 1 and 2 sold in Canada. It's being recalled because the product label...
This recall involves Siemens Dimension EXL Analyzer with LM, Dimension EXL 200 Analyzer, and Dimension RxL Max w/HM Anal...
This recall involves the BD MAX System, a medical device used in Canada. It's being recalled because it may produce fals...
This recall involves the nordicBrainEx medical device sold in Canada. It's being recalled because its power supply conta...
This recall involves Temporary Bipolar Pacing Leads sold in Canada. They are being recalled because the connector cap ma...
This recall involves Adult IV Set with Rate Flow Regulator, Rate Flow Regulator Extension Set, and Rate Flow Regulator I...
This recall involves the Access System - Cortisol Assay and UniCel DxI 600 and 800 Access Immunoassay System - Cortisol
This recall involves Kerlix 100% Bandage Cotton Large, Kerlix AMD Antimicrobial Large Roll, DERMACEA Fluff Roll, and Ker...
This recall involves Parietex Composite Parastomal Mesh sold in Canada. It's being recalled because the mesh may fail, l...
This recall involves RayStation medical device software sold in Canada. It's being recalled because of an issue with its...
This recall involves StageOne Hip Cement Spacer Molds sold in Canada. It's being recalled due to a potential commingle o...
This recall involves TEXAS Bronchoscope Tubes and Powerdrive ART1 - Tracheoscope Tubes sold in Canada. They are being re...
This recall involves the BD PCEA Administration Set sold in Canada. It's being recalled because the product has the pote...
This recall involves the Eltrac 471 II medical device sold in Canada. It's being recalled because an unreliable cable co...
This recall involves C-Section Packs sold in Canada. It's being recalled because components did not meet specifications
This recall involves the Cobas e411 Immunoassay Analyzer sold in Canada. It's being recalled because it may give inaccur...
This recall involves Honeywell Laser Aid Disposable Eyepatches sold in Canada. They are being recalled because some may
This recall involves the ARTIS pheno medical device sold in Canada. It's being recalled because a software issue may act...
This recall involves the Pruitt F3-S Polyurethane Outlying Carotid Shunt sold in Canada. It's being recalled because the...
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