Centrifuge 642 VFD Plus recall in Canada: Unauthorized device
This recall involves the Centrifuge 642 VFD Plus sold in Canada. It's being recalled because it is an unauthorized medic...
Medical device recalls in Canada cover implants, surgical equipment, and diagnostic tools. These recalls are issued by Health Canada.
4,400 recalls found
Page 91 of 220
This recall involves the Centrifuge 642 VFD Plus sold in Canada. It's being recalled because it is an unauthorized medic...
This recall involves the Atellica Ch 930 Analyzer, a medical device, sold in Canada. It's being recalled because of a so...
This recall involves the Medtronic WR9200 Wireless Recharger sold in Canada. It's being recalled because it may become u...
This recall involves the QIAcube Connect MDX, a medical device, sold in Canada. It's being recalled because a software d...
This recall involves VACUTAINER Blood Collection Tubes sold in Canada. They are being recalled because they may underfil...
This recall involves the Avelle Negative Pressure Wound Therapy Pump sold in Canada. It's being recalled because a manuf...
This recall involves the ORTHO OPTIX READER, model 6842222, sold in Canada. It's being recalled because of a software de...
This recall involves Duodenovideoscope medical devices sold in Canada. It's being recalled because deterioration of the
This recall involves Puritan Bennett 980 Series Ventilators sold in Canada. They are being recalled due to a manufacturi...
This recall involves INVACARE TDX SP2 with LINX GYRO power wheelchairs sold in Canada. It's being recalled because a sof...
This recall involves NAVICARE NURSE CALL (SOFTWARE) sold in Canada. It's being recalled because a software defect may st...
This recall involves SARS-COV-2 Rapid Antigen Test Nasal with Control kits sold in Canada. It's being recalled because s...
This recall involves several models of BIOGRAPH MCT medical devices sold in Canada. It's being recalled because improper...
This recall involves the BIOGRAPH LSO 16 SLICE PET medical device sold in Canada. It's being recalled because improper a...
This recall involves the iDESIGN Refractive Studio and related systems sold in Canada. It's being recalled because of a
This recall involves KN95 Face Masks from GUANGDONG FEI FAN MSTAR TECHNOLOGY LTD sold in Canada. They are being recalled...
This recall involves CA-N95 Flat Fold Respirators sold in Canada. They are being recalled because of a potential leak du...
This recall involves the COBAS EGFR MUTATION TEST V2 sold in Canada. It's being recalled because it may provide inaccura...
This recall involves Philips Allura Xper FD10 and FD20/10 medical devices sold in Canada. They are being recalled becaus...
This recall involves CA-N95 Flat Fold Respirators sold in Canada. It's being recalled because of labelling and packaging...
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