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Class 2 Device Recall Dialysis tubing set |
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Date Initiated by Firm |
October 24, 2005 |
Date Posted |
April 05, 2006 |
Recall Status1 |
Terminated 3 on April 17, 2012 |
Recall Number |
Z-0706-06 |
Recall Event ID |
34080 |
510(K)Number |
K011221
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Product Classification |
Dialyzer, High Permeability With Or Without Sealed Dialysate System - Product Code KDI
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Product |
Gambro Prisma HF1000 preset, Part No. 8399050. |
Code Information |
Lot number 05F0864P. Recall expanded on 04/13/2006 to include 05AXXXXX through 05J2796P |
Recalling Firm/ Manufacturer |
Gambro Renal Products, Inc. 10810 W Collins Ave Lakewood CO 80215-4439
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For Additional Information Contact |
303-231-4094
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Manufacturer Reason for Recall |
After dialysis machine is disconnected from the patient, blood leakage may occur while unloading the tubing sets from the machine.
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FDA Determined Cause 2 |
Other |
Action |
Recall information was forwarded to all Gambro Sale Organizations. Notification was sent to all US consignees on November 2nd and November 3rd, 2005. |
Quantity in Commerce |
1665 units |
Distribution |
Nationwide, including VA facilities in AZ, CA, DC, FL, GA, MI, MO, NJ, NY, OH, OR, PA, PR, TX, UT, VA, WI. Military distribution to CA and TX. Foreign distribution to Australia, Canada, Denmark, France, Germany, Hungary, UK. |
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 and Original Applicant = GAMBRO RENAL PRODUCTS
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