Yahoo Finance

Teleflex catheterization kit recall linked to 10 injuries, 1 death

Teleflex has recalled nearly 335,000 catheterization kits from the U.S. after discovering an issue linked to 10 injuries and one death, the Food and Drug Administration said Wednesday. The company ...
Becker's Hospital Review

Catheterization kits recalled after 10 injuries, 1 death: FDA

Teleflex and its subsidiary Arrow International recalled 334,995 catheter kits after receiving reports of increased resistance in the guidewire handle and chamber during use, the FDA said April 3. The ...
The Daily Star

Seniors: Watch out for catheter kit scams

The New York StateWide Senior Action Council, a 54-year-old non-profit organization dedicated to serving the needs and well-being of our State’s more than 3.6 million senior citizens, announced in a ...

Catheter Kit Billing Fraud: "The Medicare Fraud of the Month for February"

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 ...
Healio

FDA designates recall of radial artery and arterial line catheterization kits as class I

Please provide your email address to receive an email when new articles are posted on . The FDA designated the recall of radial artery and arterial line catheterization kits as class I, the most ...
Yahoo Finance

Teleflex and Arrow recall IAB catheter kits due to risk of injury or death

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, ...
Medscape

Arrow QuickFlash Radial Artery Catheterization Kits Recalled

Teleflex and its subsidiary Arrow International have recalled the Arrow QuickFlash radial artery and radial artery/arterial line catheterization kits over a potentially defective component. The ...
WTVF

FDA announces recall of balloon catheter kits

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.
FierceBiotech

Teleflex recalling aortic balloon catheter kits after reports of injuries and one death

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

FDA designates recall of central venous access, catheter kits as class I

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 ...
Healthline

Cardiac Catheterization

Cardiac catheterization is a medical procedure that cardiologists, or heart specialists, use to evaluate heart function and diagnose cardiovascular conditions. During cardiac catheterization, a long ...