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IntelliVue Patient Monitor Systems and Multi-Measurement module (2016-01-04)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2016/56750r-eng.php

Jan 22, 2016 ...-Lead ECG monitoring derivation uses a 6-lead set and derives remaining leads to provide a non-diagnostic 12-Lead view, including ECG waves and ST measurements. The ST elevation alarm on the patient monitor or stand-alone X2 measurement module will not sound when indicated for all chest leads derived using hexad 12-Lead ECG monitoring in the host monitor

Unauthorized products may pose serious health risks (October 2, 2019 to November 19, 2019)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/71157a-eng.php

Dec 9, 2019 ... nausea or vomiting; an irregular heartbeat or fluttering in the chest; feeling lightheaded when standing quickly; or unusual changes in mood or behaviour. Nandrolone decanoate is an anabolic steroid, a synthetic derivative of testosterone, and is not authorized for sale in Canada. Side effects include nausea; fluid retention with swelling of legs, feet and ankles

Safe Shopping on Black Friday and Cyber Monday

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/68332a-eng.php

Nov 21, 2018 ... on the Canadian market comply with the Canada Consumer Product Safety Act. Products are monitored for health or safety risks after they've been released onto the market, but not every product is checked or tested. To learn more about the potential risks of buying consumer products online and how you can minimize those risks, visit Buying Consumer Products Online. You can

Alcon or Endure LuxOR E71 Ophthalmic Microscope and Q-Vue Ophthalmic Microscope (2018-07-18)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/67344r-eng.php

Aug 3, 2018 ..., Healthcare Professionals, Hospitals Identification number: RA-67344 Reason Affected products Affected products Alcon or Endure LuxOR E71 Ophthalmic Microscope Alcon or Endure LuxOR E71 Q-Vue Ophthalmic Microscope Reason Through our monitoring process, Alcon has observed there is a potential for the optical head to detach from the stand on the Alcon or Endure LuxOR

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Mar 30, 2012 ... administration set to leak and/or disconnect at the bonded joint... Posted: 2019-04-28 Type of communication: Recall Important Safety Information on Alaris Infusion Sets and Alaris 8100 Pump Module - Risk of Over-Infusion Health Canada’s ability to monitor the safety of marketed health products depends on healthcare providers and consumers reporting adverse reactions

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=9000&plain_text=&s=

Mar 30, 2012 ... in the "indications" section. The indications incorrectly states, "Silane is intended to be used as a coupler between the prepared tooth and the cement on the restoration." the correct... Posted: 2014-11-20 Type of communication: Recall Heartstart MRx Defibrillator/Monitor (2014-11-20) Heartstart MRx Defibrillator/Monitor (2014-11-20) Recalled Products Heartstart MRx

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=10000&plain_text=&s=

Mar 30, 2012 ...Search interface for Health Canada website

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=11000&plain_text=&s=

Mar 30, 2012 ...: 11001-12000 of 30602 Previous Next Heartstart MRX Defibrillator / Monitor (2014-02-24) Heartstart MRX Defibrillator / Monitor (2014-02-24) Recalled Products Heartstart MRX Defibrillator / Monitor Philips has become aware that when used in hospital transport and pre-hospital (EMS) environments, the connection between the pads/paddles therapy cable (including pads

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=6000&plain_text=&s=

Mar 30, 2012 ... SYSTEM - HYBRID & RESCUE INTRA-AORTIC BALLOON PUMP (2016-04-05) CARDIOSAVE SYSTEM - HYBRID & RESCUE INTRA-AORTIC BALLOON PUMP (2016-04-05) Affected products A. CARDIOSAVE SYSTEM - HYBRID & RESCUE INTRA-AORTIC BALLOON PUMP Maquet continually monitors the performance of the CARDIOSAVE IABPs and has discovered four issues that could affect the CARDIOSAVE IABP

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=8000&plain_text=&s=

Mar 30, 2012 .... ... Posted: 2015-05-07 Type of communication: Recall Expression MRI Patient Monitoring System-Main Unit (2015-05-07) Expression MRI Patient Monitoring System-Main Unit (2015-05-07) Recalled Products Expression MRI Patient Monitoring System-Main Unit Philips has become aware that recent revisions of the device's Instructions for Use (IFU) (part number 989803162691

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