Date Initiated by Firm |
December 15, 2005 |
Date Posted |
February 04, 2006 |
Recall Status1 |
Terminated 3 on January 26, 2012 |
Recall Number |
Z-0474-06 |
Recall Event ID |
34380 |
510(K)Number |
K011342
|
Product Classification |
Counter, Differential Cell - Product Code GKZ
|
Product |
COULTER LH 700 Series Hematology Analyzer, PN 6605632 and 6605632R
|
Code Information |
PN 6605632 and 6605632R All Software Versions |
Recalling Firm/ Manufacturer |
Beckman Coulter Inc 200 S Kraemer Blvd Brea CA 92822-6208
|
For Additional Information Contact |
Nora Zerounian 714-961-3634
|
Manufacturer Reason for Recall |
There is a risk of sample misidentification when processing samples in the Manual aspiration mode.
|
FDA Determined Cause 2 |
Other |
Action |
A Product Corrective Action letter will be mailed the week of Dec 19, 2005 to all COUL TER@ LH700 Series System & COUL TER@ GEN.STM System customers instructing them of a rare risk of sample misidentification. (Letter will be sent by US mail) |
Quantity in Commerce |
1715 |
Distribution |
Nationwide and Canada |
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.
|
510(K) Database |
510(K)s with Product Code = GKZ and Original Applicant = BECKMAN COULTER, INC.
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