The StateWide Fraud of the Month is a component of the Senior Medicare Patrol (SMP), the definitive resource for New York State's older adults and caregivers to detect, prevent, and report healthcare ...

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 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.

Struggling Teleflex ($TFX) in February warned of an impending restructuring plan that will involve the usual mix of layoffs, relocations and outsourcing. The Wayne ...

The U.S. Food and Drug Administration has classified a recall by Merit Medical Systems Inc. MMSI as its most serious type, ...

According to the latest market analysis by Future Market Insights, the global central venous catheter market is witnessing ...

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 ...

Please provide your email address to receive an email when new articles are posted on . The recall of two varieties of intra-aortic balloon catheter kits has been ...

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 ...

July 24, 2006 — The US Food and Drug Administration (FDA) and Medtronic, Inc, have warned healthcare professionals via letter regarding the worldwide voluntary recall of nonimplanted intrathecal ...

Pulmonary-artery catheterization aids the diagnosis and management of numerous cardiovascular illnesses, including pulmonary hypertension, cardiogenic shock, mixed shock states, cardiac tamponade, and ...