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Central Alerting System: Cardiac Pacemaker Failure

by admin | 26/02/2019 | Archive, CAS Alert

Source: Medicines & Healthcare products & Regulatory Agency (MHRA)   Summary On the 13th of February 2019, MHRA issued a Medical Device Alert for Implantable Cardiac Pacemakers manufactured by Medtronic Inc. The alert is in regards to a subset of dual...

Central Alerting System: Drug Alert Class 2 Medicines Recall

by admin | 26/02/2019 | Archive, CAS Alert

Source: Medicines & Healthcare products & Regulatory Agency (MHRA)   Summary On the 13th of February 2019, MHRA issued a Class 2 Medicines Recall for the  Irbesartan 300mg Film-Coated Tablets; Irbesartan and the  Hydrochlorothiazide 300 / 25mg Film-Coated...

Central Alerting System: Professional Use Monitor/Defibrillator Device Failure

by admin | 26/02/2019 | Archive, CAS Alert

Source: Medicines & Healthcare products & Regulatory Agency (MHRA)   Summary On the 20th of February 2019, MHRA issued a medical device alert for the professional use monitor/defibrillator: LIFEPAK 15 manufactured by Stryker. The alert is in regards to...

Risk Of Spreader Bar Detachment From Portable Lifts Without A Scale

by admin | 01/02/2019 | CAS Alert

Source: Central Alerting System (CAS) Summary On the 30th of January 2019, CAS issued a medical device alert for the Arjo Minstrel Passive Floor Life, manufactured by ArjoHuntleigh AB. The alert is in regards to the spreader bar that may detach from the lift arm...

Nellix Endovascular Aneurysm Sealing (Evas) System – Device Recall & Enhanced Patient Surveillance

by admin | 01/02/2019 | Archive, CAS Alert, Updates

Source: Central Alert System (CAS) Endologix has stopped selling the Nellix EVAS device and is recalling unused stock. MHRA recommends enhanced patient surveillance due to a high risk of graft failure beyond two years after implantation. These are the following...
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