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Terminated

COULTER LH 750 and LH 780 Analyzers. The COULTER LH 750 Hematology Analyzer is a quantitative, automated hematology analyzer and leukocyte differential counter For In Vitro Diagnostic Use in clinical laboratories. The COULTER LH 750 Hematology Analyzer provides automated Reticulocyte analysis and enumeration of nucleated red blood cells (NRBCs) as well as an automated method for enumeration of RBCs and WBCs in body fluids. The COULTER LH 780 Hematology Analyzer is a quantitative, automated hematology analyzer and leukocyte differential counter For In Vitro Diagnostic Use in clinical laboratories. The COULTER LH 780 Hematology Analyzer also provides automated Reticulocyte analysis and enumeration of nucleated red blood cells (NRBCs) as well as an automated method for enumeration of RBCs and WBCs in body fluids.

FDA Recall Z-0113-2014 · Posted 2013-11-01

Recalling FirmBeckman Coulter Inc.
Recall StatusTerminated
Product CodeGKZ
Date Initiated2013-09-24
Date Terminated2014-10-09
Product Quantity1,697 units

Reason for Recall

The check valves may fail on the Coulter LH 750 Hematology Analyzer (PN 6605632 and A85570) and Coulter LH 780 Hematology Analyzer (PN 723585 and A90728). A failure may result in an air or liquid leak at the connection to the Vacuum Overflow Tank waste line or at the Backwash Tank drain line.

Firm Action

Beckman Coulter sent a Urgent Product Correction letter dated September 12, 2013, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. . The customer notification letter dated September 12, 2013, titled "URGENT PRODUCT CORRECTION", provided product description with codes, the issue (reason for recall), impact, action, resolution, and contact information. Customers were instructed to: If you experience a "Backwash Tank Not Full" error message, review manual mode sample results since the last acceptable QC run. System safeguards that assist with detection of erroneous results include Startup, QC, system messages and flagging (e.g., R), delta checks, flagging from limit sets (H, L, a, c), definitive messages and decision rules that would trigger further review. Avoid physical contact with a possible leak by continuing to use personal protective equipment as recommended in the Instructions for Use and by national regulations. If you have any questions concerning this notification, please contact our Customer Support Center: Via our website, http://www.beckmancoulter.com/customersupport/support Via phone, call 800-526-7694 in the United States and Canada. Outside US and Canada, contact your local Beckman Coulter Representative We apologize for the inconvenience this issue has caused your laboratory.

Root Cause

Component change control

Distribution Pattern

Worldwide Distribution - Nationwide Distribution and the country of Canada..

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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