FDA Recall - Fresenius HD Products

If you’re using any of these items that have been recalled, talk with your home training nurse. Here’s the link to the section of the recall notice about Fresenius products that I copied and pasted below:
http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm224723.htm

RECALLS AND FIELD CORRECTIONS: DEVICES - CLASS II


PRODUCT

  1. Fresenius 2008H Dialysate Delivery Machine, Catalog numbers 501228, R190188 (Refurbished), R501228, RTLR501228 (Refurbished). Recall # Z-2224-2010;

  2. Fresenius 2008K, 2008K2 and 2008 K2@home Hemodialysis Machines, Catalog numbers: 2008K: 190300, 190303, 190305, 190336, 190371, 190372, 190373, 190517, R190305 (Refurbished), R190371 (Refurbished), RTL190371, RTL190373, RTLR190305 (Refurbished), RTLR190371 (Refurbished), RTLR190373 (Refurbished).
    Recall # Z-2225-2010;

  3. Fresenius Granuflo 1 Mixer Dissolution Unit - Tested, and Granuflo Dissolution Tank, Model Numbers G047-80101 and RTLG047-80101, Catalog Numbers G047-80101 and RTLG047-80101. Recall # Z-2226-2010;

  4. Main Power Supply Assembly (50 and 60 Hz) and AC Power cord assembly for hemodialysis machines and Granuflo 1 mixers. Catalog Numbers 190011 (60 Hz main power supply), 190092 (50 Hz main power supply), 150425 (AC power cord assembly -hemodialysis machine) and 160089 (AC power cord assembly, Granuflo 1 mixers). Recall # Z-2227-2010
    CODE
    No lot numbers
    RECALLING FIRM/MANUFACTURER
    Recalling Firm: Fresenius Medical Care North America, Waltham, MA, by letter on June 28, 2010.
    Manufacturer: Fresenius USA, Inc., Walnut Creek, CA. Firm initiated recall is ongoing.
    REASON
    Power cords may fail if the prongs crack or fail at the plug, and may become a fire/burn/shock hazard or delay/interrupt therapy.
    VOLUME OF PRODUCT IN COMMERCE
    72,142 units
    DISTRIBUTION
    Nationwide and Internationally