| Class 2 Device Recall Phoenix Hemodialysis Delivery System | |
Date Initiated by Firm | September 10, 2007 |
Date Posted | March 25, 2008 |
Recall Status1 |
Terminated 3 on January 03, 2012 |
Recall Number | Z-1367-2008 |
Recall Event ID |
45950 |
510(K)Number | K001156 |
Product Classification |
Dialysis system - Product Code KDI
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Product | Gambro cartridge blood tubing set used with Gambro Dasco Phoenix and Cobe Centrysystem 3 (and 3+) Hemodialysis System, Gambro, Lakewood, CO 80401 |
Code Information |
All catalog numbers involving the Gambro Cartridge Blood Sets: 003409-400, 003409-410, 003410-500, 003410-510, 004310-710, 003411-500, 003412-500, 003414-500, 003414-510, 003415-510, 003422-500, 003422-515, 003422-520, 003429-500. |
Recalling Firm/ Manufacturer |
Gambro Renal Products, Inc. 14143 Denver West Pkwy Lakewood CO 80401-3116
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For Additional Information Contact | 303-231-4094 |
Manufacturer Reason for Recall | Kinked tubing on hemodialysis device may cause hemolysis. |
FDA Determined Cause 2 | Device Design |
Action | On September 10, 2007, the firm sent an Advisory Notice to all consignees alerting them that a kink in the tubing can result in physical hemolysis. The firm included with the Notice a Quick Reference Guide that provides drawing of the proper installation of the Phoenix and describes how to prevent bloodline kinking. A customer reply form was also included. The firm is in the process of making labeling changes that will be released with the updated software revisions. |
Quantity in Commerce | 41,000,000 |
Distribution | Nationwide, including 17 VA facilities and 1 military facility. Foreign distribution to Canada, Korea, Mexico. |
Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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510(K) Database | 510(K)s with Product Code = KDI
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