Recall: Health Canada Warns of Medical Devices Potentially Causing Death

Health Canada has issued a series of recalls for various medical devices, citing potential risks that could harm patients. Among the affected devices is the OmniLab Advanced, commonly used by individuals with sleep apnea, a condition where breathing stops and starts during sleep. Health Canada warns that the device could experience internal errors or problems, leading to interruptions in therapy that may result in serious health complications, including respiratory failure or even death in vulnerable patients.

In addition to the OmniLab Advanced, Health Canada has recalled multiple Medtronic cannulae products due to a potential sterility breach. These products, such as cardiac suction tubes and Arteriotomy Cannulae, are used for various medical procedures involving fluid drainage, medication administration, and oxygen or blood provision.

One specific device, the Hugo Ras Surgeon Console, used for robotic assistance during surgeries, is also subject to a recall. The agency identified incidents of power loss from the main supply, which could prevent surgeons from teleoperating the system before or during procedures, posing serious risks to patients.

Furthermore, several models of ophthalmic surgery procedure packs have been recalled due to concerns about inflammation and ocular tissue damage. The use of these recalled products could lead to temporary or reversible adverse health effects, prompting Health Canada to take action to safeguard patient well-being.

Additionally, Medline Industries and Lp have issued a recall for their paracervical/pudendal kits, as the ring on the trumpet needle guide may detach under excessive pressure. These recalls underscore the importance of ensuring the safety and effectiveness of medical devices to protect patients from potential harm.

Individuals who have used any of the recalled devices are advised to contact the manufacturers for further information. These recalls serve as a reminder of the critical role regulatory agencies play in monitoring and addressing potential risks associated with medical devices to safeguard public health and safety.