Nitinol Devices and Components HydroFinity Hydrophilic guidewire recall — FDA Z-1815-2014
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Overview of recall records associated with Nitinol Devices and Components, Inc., including dates, categories and classifications where available.
Classification mix: Class I: 12.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
This page summarizes recall records in which the official source identifies Nitinol Devices and Components, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.