Z-1818-2014 Class I Terminated
Recall Details
- Product Type
- Devices
- Report Date
- July 2, 2014
- Initiation Date
- May 28, 2014
- Termination Date
- January 13, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 8485 in US, 9595 - ROW - total, all models
Product Description
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled Tip, 150 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures.
Reason for Recall
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Distribution Pattern
Worldwide Distribution - USA (nationwide) and Internationally to Italy, France, Norway, Sweden, Germany, Belgium, United Kingdom and Canada.
Code Information
Model HPSA35150- all lots.