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U.S. Department of Health and Human Services

Class 2 Device Recall

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  Class 2 Device Recall see related information
Date Initiated by Firm October 07, 2003
Date Posted July 20, 2004
Recall Status1 Terminated 3 on August 30, 2004
Recall Number Z-1116-04
Recall Event ID 29117
510(K)Number k965240  k014034  k011213  k023049  
Product Synchron LX Clinical Systems Software
Code Information All Software versions.
Recalling Firm/
Manufacturer		 Beckman Coulter Inc
200 S Kraemer Blvd
Brea CA 92822-6208
Manufacturer Reason
for Recall		 'Initial Rate High' parameter for User Defined Reagents does not perform as indicated in the Synchron LX Clinical Systems Operations Manual.
FDA Determined
Cause 2		 Other
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 = and Original Applicant = BECKMAN COULTER, INC.
510(K)s with Product Code = and Original Applicant = BECKMAN INSTRUMENTS, INC.
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