Alinity ci-Series System Control Module (2020-06-26)
This recall involves the Alinity ci-Series System Control Module sold in Canada. It's being recalled because of issues w...
Medical device recalls in Canada cover implants, surgical equipment, and diagnostic tools. These recalls are issued by Health Canada.
4,400 recalls found
Page 124 of 220
This recall involves the Alinity ci-Series System Control Module sold in Canada. It's being recalled because of issues w...
This recall involves the CARESCAPE ONE medical device sold in Canada. It's being recalled because it may not alarm for a...
This recall involves Active Cord medical devices sold in Canada. It's being recalled because cord damage could cause spa...
This recall involves the ACTIV.A.C Therapy Unit sold in Canada. It's being recalled because the unit may shut down witho...
This recall involves Anti Flu Reusable Protective KN95 N95 Face Masks sold in Canada. They are being recalled because th...
This recall involves Gibco Gurr Buffer Tablets sold in Canada. They are being recalled because the tablets are one tenth...
This recall involves Thoracentesis/Paracentesis Trays sold in Canada. They are being recalled because the drainage set m...
This recall involves 3-PLY DISPOSABLE BLUE FACE MASKS imported by SOBEZONE INC and manufactured by HUBEI KIMSOUL INDUSTR...
This recall involves the Neurosign V4 Intra-operative Nerve Monitor sold in Canada. It's being recalled because manipula...
This recall involves the Prompt Inoculation System-D Inoculation Wand sold in Canada. It's being recalled because some b...
This recall involves the Ultimax-i medical device sold in Canada. It's being recalled because images acquired by the dev...
This recall involves certain lots of LoFric Origo urethral catheters sold in Canada. They are being recalled due to a po...
This recall involves the VNS Therapy Programming Software Model 3000 1.6 used in Canada. It's being recalled because it
This recall involves KN95 Face Masks sold in Canada. They are being recalled because they failed to meet the 95% filtrat...
This recall involves Sterile Solution Media Transport Tubes sold in Canada. They are being recalled because of a potenti...
This recall involves the DxA 5000 medical device sold in Canada. It's being recalled because confusing instructions for
This recall involves Elekta Unity and Philips Marlin Software used in medical devices in Canada. It's being recalled bec...
This recall involves KN95 Face Masks sold in Canada. They are being recalled because they do not meet filtration require...
This recall involves Skaffold Next Generation Bone Void Filler 5CC and 10CC sold in Canada. It's being recalled because
This recall involves TEM Insufflation Tubing sold in Canada. It's being recalled because the hose material does not meet...
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