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Avalon Fetal Monitor - Risk of Inaccurate Ultrasound-Derived Fetal Heart Rate Monitoring

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/71217a-eng.php

Oct 9, 2019 ...Avalon Fetal Monitor - Risk of Inaccurate Ultrasound-Derived Fetal Heart Rate Monitoring Report a Concern Starting date: October 9, 2019 Posting date: October 9, 2019 Type of communication: Dear Healthcare Professional Letter Subcategory: Medical Device Source of recall: Health Canada Issue: Important Safety Information Audience: Healthcare Professionals

Single Patient Use Lead Set (2019-09-03)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/71131r-eng.php

Oct 3, 2019 ...Single Patient Use Lead Set (2019-09-03) Report a Concern Starting date: September 3, 2019 Posting date: October 3, 2019 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type III Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare Professionals, Hospitals Identification

ApexPro Telemetry System (2019-09-09)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/71025r-eng.php

Sep 20, 2019 ...ApexPro Telemetry System (2019-09-09) Report a Concern Starting date: September 9, 2019 Posting date: September 20, 2019 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare Professionals, Hospitals Identification

Brilliance 40-64 Slice CT System, Brilliance ICT System - System, Brilliance ICT SP System - Main, Ingenuity CT System (2019-06-25)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70453r-eng.php

Jul 19, 2019 ...Brilliance 40-64 Slice CT System, Brilliance ICT System - System, Brilliance ICT SP System - Main, Ingenuity CT System (2019-06-25) Report a Concern Starting date: June 25, 2019 Posting date: July 19, 2019 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II Source of recall: Health Canada Issue: Medical

ECG Leads and Cables, ECG Trunk Cables (2019-05-15)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70067r-eng.php

May 31, 2019 ...ECG Leads and Cables, ECG Trunk Cables (2019-05-15) Report a Concern Starting date: May 15, 2019 Posting date: May 31, 2019 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare Professionals, Hospitals Identification

MAC VU360 (2019-06-28)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70417r-eng.php

Jul 15, 2019 ...MAC VU360 (2019-06-28) Report a Concern Starting date: June 28, 2019 Posting date: July 15, 2019 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare Professionals, Hospitals Identification number: RA-70417 Last

Xper Flex Cardio Physiomonitoring System-Main Unit (2018-11-18)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/68468r-eng.php

Dec 3, 2018 ...Xper Flex Cardio Physiomonitoring System-Main Unit (2018-11-18) Report a Concern Starting date: November 18, 2018 Posting date: November 30, 2018 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare Professionals

IsoAir Mattress

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/62660r-eng.php

Mar 16, 2017 ... Affected products Reason Stryker is the distributor of the IsoAir system. The specification developer/manufacturer of the IsoAir system has determined that electrical interference emanating from the system may cause clinically unacceptable levels of signal artifact in electrophysiological monitoring devices, e.g. ECG, EKG or EEG. This only occurs when the active

Symbia Evo Excel (2018-10-09)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/68228r-eng.php

Nov 16, 2018 ...Symbia Evo Excel (2018-10-09) Report a Concern Starting date: October 9, 2018 Posting date: November 15, 2018 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type III Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare Professionals, Hospitals Identification number: RA

Heartstart XL, Heartstart MRX Defibrillator/Monitor and Heartstart XL+ (2018-04-18)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/66814r-eng.php

May 18, 2018 ...Heartstart XL, Heartstart MRX Defibrillator/Monitor and Heartstart XL+ (2018-04-18) Report a Concern Starting date: April 18, 2018 Posting date: May 18, 2018 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare

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