Atlas FDA

Coulter LH 750 Hematology Analyzer, Part No. 6605632, A85570 Product Usage: The Coulter LH 750 Hematology Analyzer is a

FDA device recall Z-0470-2014 · posted 2013-12-10 · Terminated

Recall details

Recalling firm
Beckman Coulter Inc.
Reason for recall
Beckman Coulter is recalling the LH 750 and LH 780 Hematology Systems because the optical degradation may potentially cause a delay in reporting results for nucleated red blood cells (nRBC), white blood cell differential and/or reticulocytes.
Action taken
Beckman Coulter sent an customer notification letter dated 11/8/13 to all customers who purchased the LH 750 and LH 780 Hematology Systems. The letter informs the customers of the problems identified and the actions to be taken. Customers are instructed to complete and return the enclosed response form within 10 days. Customers with questions are instructed to contact Beckman Coulter's Customer Support Center at http://www.beckmancoulter.com/customer/support or call (800) 526-7694 in the US and Canada. Outside the US and Canada, customers are instructed to contact Beckman Coulter Representative. On 2/17/14, Beckman Coulter expanded the recall to inform Coulter LH 750 and Coulter LH 780 Hematology Analyzer customers of the issue related to LH Cleaner and Coulter Clenz.
Root cause
Under Investigation by firm
Status
Terminated
Product code
GKZ
Quantity affected
4155 units total (1676 units in US)
Distribution
Worldwide Distribtion - USA Nationwide including the countries of Algeria, Andorra, Angola, Australia, Austria, Bahrain, Bangladesh, Belgium, Bermuda, Bosnia and Herzegovina, Bulgaria, China, Colombia
Date initiated
2013-11-08
Date posted
2013-12-10
Date terminated
2014-12-25
Location
Brea, CA

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Related 510(k) clearances

RecordFirmDate
COULTER LH 750 HEMATOLOGY ANALYZER, MODEL 6605632 (K011342)Beckman Coulter, Inc.2001-07-09