News | Angiographic Catheter | July 25, 2016

Stryker Sustainability Solutions Recalls Angiodynamics Soft Vu Omni Flush Angiographic Catheters

Company has received reports of catheter tip separating from the main body, leading to a loss of device function and other complications

Stryker Sustainability Solutions, Angiodynamics Soft Vu Omni Flush Angiographic Catheters, recall

July 25, 2016 — Stryker Sustainability Solutions (formerly Ascent Healthcare Solutions) is recalling Angiodynamics Soft Vu Omni Flush Angiographic Catheters due to reports of separation of the tip of the catheter from the main body. Tip separation leads to loss of device function, possible surgical intervention to retrieve a separated segment, or other complications such as blocking blood flow to bodily organs.

Tip separation can also lead to internal organ injury and cause stroke, kidney failure and intestinal failure among other serious adverse health consequences, including death.

The recalled products include manufacturing dates Nov. 7, 2003 to Oct. 18, 2008, and distribution dates Jan. 5, 2004 to Dec. 3, 2008.

The Soft-Vu Omni Flush Angiographic Catheter is used to inject contrast dye into blood vessels in preparation for a cardiac angiogram, a type of X-ray used to diagnose heart conditions. The catheter is inserted into the body through a small puncture made in the skin and into a blood vessel.

On June 1, 2016, Stryker Sustainability Solutions sent a Customer Notification letter to customers informing them of the high possibility of tip separation during use. The letter also asked customers to:

  • Discontinue use of the affected lots of the recalled products;
  • Check their inventories for affected lots of the unused products;
  • Ship all affected products found back to Stryker; and
  • Acknowledge receipt of the letter by returning the enclosed Device Recall Effectiveness Check form by postal mail, or by contacting their Stryker Sustainability Sales Representative by email.

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the U.S. Food and Drug Administration’s (FDA) MedWatch Safety Information and Adverse Event Reporting Program.

For more information:

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