BEUDAMED
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    SteriLyte Liquid Bicarbinate, Formula CL-02; 1 gallon (3.78 L); manufactured by Rockwell Medical Technologies, Inc., Grapevine, TX 76051. This product is used in conjunction with C-Series RenalPure Liquid Acid Concentrate or DC-Series Dri-Sate Dry Acid Concentrate in artificial kidney (hemodialysis) machines.

    FDA Recall
    Terminated ·Rockwell Medical Technologies, Inc·Product code KPO·September 29, 2008

    SteriLyte Liquid Bicarbinate, Formula RL-01; 1 gallon (3.78 L); manufactured by Rockwell Medical Technologies, Inc., Grapevine, TX 76051. This product is used in conjunction with C-Series RenalPure Liquid Acid Concentrate or DC-Series Dri-Sate Dry Acid Concentrate in artificial kidney (hemodialysis) machines.

    FDA Recall
    Terminated ·Rockwell Medical Technologies, Inc·Product code KPO·September 29, 2008

    RenalPure Liquid Acid Concentrate R-006; One Gallon (3.78 liters); manufactured by Rockwell Medical Technologies, Inc., Grapevine, TX 76051.

    FDA Recall
    Terminated ·Rockwell Medical Technologies, Inc·Product code KPO·December 3, 2007

    RenalPure Liquid Acid Concentrate R-235; One Gallon (3.78 liters); manufactured by Rockwell Medical Technologies, Inc., Grapevine, TX 76051.

    FDA Recall
    Terminated ·Rockwell Medical Technologies, Inc·Product code KPO·December 3, 2007

    RenalPure Liquid Acid Concentrate R-259; One Gallon (3.78 liters); manufactured by Rockwell Medical Technologies, Inc., Grapevine, TX 76051.

    FDA Recall
    Terminated ·Rockwell Medical Technologies, Inc·Product code KPO·December 3, 2007

    Glacial Acidic Acid (liquid component of Dri-Sate Dry Acid Concentrate DR-215); 1 quart (0.95 liters); manufactured by Rockwell Medical Technologies, Inc., Grapevine, TX 76051.

    FDA Recall
    Terminated ·Rockwell Medical Technologies, Inc·Product code KPO·December 3, 2007

    Dri-Sate Glacial Acidic Acid (liquid component of Dri-Sate Dry Acid Concentrate DR-240); 1 quart (0.95 liters); manufactured by Rockwell Medical Technologies, Inc., Grapevine, TX 76051.

    FDA Recall
    Terminated ·Rockwell Medical Technologies, Inc·Product code KPO·December 3, 2007