Please provide your email address to receive an email when new articles are posted on . The FDA announced that Teleflex and Arrow International LLC are recalling both the Arrow MAC Two-Lumen Central ...
Teleflex and its subsidiary Arrow International have initiated a recall of specific intra-aortic balloon (IAB) catheter kits due to a manufacturing defect that may prevent full balloon inflation, ...
Struggling Teleflex ($TFX) in February warned of an impending restructuring plan that will involve the usual mix of layoffs, relocations and outsourcing. The Wayne ...
Teleflex is recalling International Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits, according to an FDA press release on Friday. The recall is considered by the FDA as a Class 1.
DUBLIN, April 27, 2021 /PRNewswire/ -- Medtronic plc (NYSE:MDT), the global leader in medical technology, today announced it has received Breakthrough Device Designation status from the U.S. Food and ...
OKLAHOMA CITY (KFOR) – The Oklahoma Insurance Department (OID)’s Medicare Assistance Program (MAP) is warning about rising cases of Medicare fraud across the state, including beneficiaries being ...
The new Hemolung XG4 Cartridge and Catheter Kits further simplify initiation of Respiratory Dialysis ®. PITTSBURGH--(BUSINESS WIRE)--ALung Technologies, Inc., the leading provider of low-flow ...
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