ClearanceBrief
Recall Z-0440-2009 ยท KPO Dialysate Concentrate For Hemodialysis (Liquid Or Powder)

Rockwell Medical Technologies, Inc

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.

DateJan 5, 2009 (initiated Sep 29, 2008)
StatusTerminated
ReasonMicrobial growth was observed in the retain samples of 4 lots of Liquid Bicarbonate after products had been distributed.
Root causeEnvironmental control
ActionRecall notification was faxed and/or e-mailed to consignees on 09/29/08 and then sent via mail on 09/30/08. A follow-up response form was faxed to consignees starting 10/01/08. Consignees asked to return product for a credit. For additional information, contact Rockwell Medical Technologies, Inc., Customer Service at 1-800-449-3353.
Quantity695 cases (4 units per case)
DistributionNationwide. Product distributed to AL, AR, FL, GA, NC, SC, TN, TX, and VA.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K022521BICARBONATE DIALYSATE CONCENTRATE MIXER, MODEL 50 GALLON & 100 GALLON
Rockwell Medical Technologies, Inc., Jan 3, 2003