FDA Announces Class I Recall On Arrow International Cardiac Catheter Device
The US FDA has announced a high-risk class I recall on a cardiac catheter from Teleflex Inc. subsidiary Arrow International due to the risk of tip damage during use.
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The US FDA has designated a recall of nearly 2,000 cardiovascular catheter kits from Teleflex subsidiary Arrow International class I, its most serious type.
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News We’re Watching: CDRH’s Maisel Announces Retirement, Fresenius Clearance, Philips and Smiths Recalls
This week, a device center stalwart prepared to say goodbye; the FDA cleared Fresenius's 5008X Hemodialysis System; and class I recalls for Smiths Medical and Philips Imaging were announced.