Medical device and MedTech insights, news, tips and more

Stryker Voluntarily Recalled 167 Angiographic Catheters 

July 29, 2016

angiographic catheters

Stryker Sustainability Solutions voluntarily recalled 167 of its Angiodynamics Soft Vu Omni Flush angiographic catheters.

angiographic catheters

The company received reports of the tip of the catheter separating from the main body, which could lead to loss of device function, surgical intervention or other complications. The tip separation can also cause organ injury, stroke, kidney failure, intestinal failure and death in some circumstances, according to an FDA release on July 22.

Healthcare professionals use the catheters to inject dye into the blood vessels to prepare for a cardiac angiogram. They insert the catheters through a small skin puncture and into a blood vessel.

The recalled products were manufactured from Nov. 7, 2003, to Oct. 18, 2008, and distributed from Jan. 5, 2004, to Dec. 3, 2008.

Stryker recalled devices in Texas, Utah, Pennsylvania, California, Vermont, Maine, Washington, Virginia, New York, Maryland and Connecticut.

Read Full Article – Source: Stryker recalls 167 angiographic catheters | Cardiovascular Business

By Tim Casey

More insights

November 11, 2024
What is the Difference Between MedTech and TechMed?  
Learn More
March 7, 2024
FDA Clears Dexcom’s First Over-the-Counter Continuous Glucose Monitor
Learn More
March 1, 2024
FDA greenlights Boston Scientific’s Novel Drug-Coated Balloon for Coronary In-Stent Restenosis
Learn More

Begin your legacy now. We are your medtech and medical device talent advisory firm.