APC recall gets to the core of pacemaker shutdowns
This article was originally published in Clinica
Executive Summary
UK company APC Medical is recalling certain batches of its 4170 single-chamber external Temporary Cardiac Pacemaker to perform modifications that it hopes will solve the device's shutdown problems, reported in April 2004. An investigation of the affected devices has not revealed the root cause of the problem, but there is evidence that electromagnetic interference at certain frequencies could be to blame.
You may also be interested in...
Alvotech Highlights Lack Of Simponi Rivals As It Delivers Golimumab Results
Alvotech has just become the first company to announce positive topline results from a confirmatory clinical study for a proposed golimumab rival to Simponi and Simponi Aria – and moreover, the firm sees limited competition from other biosimilars on the horizon.
Xbrane Assembles The Troops As FDA Says No To Lucentis Biosimilar
Xbrane Biopharma was riding the crest of a wave with the EU launch of its biosimilar to Lucentis, following years of toil and investment. However, plans to roll out the product in the US will have to be pushed back – likely – into the middle of 2025, following a US FDA complete response letter.
UK MHRA Updates Assistive Tech And Borderline Regulations
Device classification themes were uppermost in April for the UK regulator, which issued key guidance in two areas prone to complexities. It also contributed to the MedTech Directorate’s one-year progress report.