Thursday, May 26, 2022

Abbott Recalls Dragonfly OpStar Imaging Catheter for Loose Marker Band That May Cause Patient Harm

Serious injuries or death may result from the use of these devices. This is a Class I recall, the most serious type of recall.

If your email program has trouble displaying this email, view as a webpage.

CDRH Medical Device Recall

Bookmark and Share

Abbott Medical Recalls DragonFly OpStar Imaging Catheter for Potential Loose Catheter Marker Band That May Cause Patient Harm

Abbott is recalling certain lots of the Dragonfly OpStar imaging catheter with optical coherence tomography (OCT) imaging system because the marker band farthest from the catheter tip (proximal marker) may become loose and/or separate from the catheter. A loose marker band could separate from the device and remain in the body after the catheter is removed, potentially leading to blood vessel (vascular) damage and/or other patient harm.

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries, serious health consequences, or death.

Read More

Questions?

Customers with questions or concerns about this recall should contact their local Abbott representative or call the customer service department at 800-227-9902.


This email was sent to ooseims.archieves@blogger.com using GovDelivery Communications Cloud on behalf of: U.S. Food and Drug Administration · 
10903 New Hampshire Ave · Silver Spring, MD ·  20993-0002 ·  1-888-INFO-FDA
GovDelivery logo

No comments:

Post a Comment