Health Canada Issues Recall of Glucose Monitors Over Risks

Health Canada has announced a recall of certain glucose monitors due to potential inaccuracies in readings that could adversely affect individuals with diabetes. The recall specifically targets the FreeStyle Libre 3 Plus Sensors, with the affected serial numbers being T60003522 and T60003216, as well as the model number 78791-01.

The agency emphasizes that these monitors may inaccurately report low glucose levels. Such erroneous readings can lead users to make unsafe treatment decisions. For instance, individuals might consume excessive carbohydrates or delay necessary insulin doses, both of which could result in serious health consequences, including injury or even death.

According to Health Canada, users are urged to verify the serial number on their glucose monitors to determine if their device is included in the recall. For those possessing a recalled model, the agency advises immediate cessation of use. Users should dispose of the device responsibly and request a replacement from the manufacturer.

The recall highlights the critical importance of accurate glucose monitoring for diabetes management. Individuals relying on these devices must ensure they are using models that function correctly to avoid potentially life-threatening situations. Health Canada’s proactive measure aims to safeguard the health of the diabetes community and prevent adverse outcomes related to incorrect glucose readings.

As part of its ongoing commitment to public safety, Health Canada will continue to monitor the situation and provide updates as necessary. Users and healthcare providers are encouraged to stay informed and report any issues they may encounter with their glucose monitoring devices.