Medical Device Safety and Recalls: HydroFinity Hydrophilic Guidewire

["U.S. Food & Drug Administration (FDA)" <fda@xxxxxxxxxxxxxxxxxxxxxxx>]

Title: Medical Device Safety and Recalls: HydroFinity Hydrophilic Guidewire

A recall has been issued for all lots of the HydroFinity Hydrophilic Guidewire because it may be damaged during use which could lead to injury.  This device is used to place catheters and other diagnostic devices during invasive medical procedures. For more information, please see http://www.fda.gov/MedicalDevices/Safety/ListofRecalls/ucm402724.htm

---

Subscriber Services:
Manage Preferences  |  Unsubscribe  |  Help with this service

Stay Connected:

Excellent customer service is important to us. Please take a moment to provide feedback regarding the customer service you have received by taking our Customer Service Survey.

---

This email was sent to list-fda@xxxxxxxxxxx using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420