Suspending your cells in a solution that is also hazardous, you need to write that information on the waste card as well – every time you use the cell counter. As for the instrument reagents, these will be ordered from Beckman Coulter by the lab manager and stocked near the instrument.

BECKMAN COULTER, INC. COULTER® LH500 HEMATOLOGY ANALYZER DIFFERENTIAL CELL COUNTER Model Number LH500 Event Date  Event Type Malfunction Manufacturer Narrative Event Description A customer reported manual mode issues on coulter lh500 hematology analyzer. The customer reported that diluent leaked into the secondary probe causing a patient sample to become diluted. The volume of the leak was approximately 250 ul and the leak was contained in the microtainer specimen tube. Low white blood cell, red blood cell, hemoglobin, hematocrit, mean corpuscular volume, and platelet results were obtained on the diluted sample, without instrument generated flags, as compared to the recollected sample which was analyzed on another hematology instrument and which was considered correct. The erroneous results were not reported out of the laboratory, and there was no change to patient treatment. The customer was wearing a lab coat and gloves when the leak was discovered.

There was no report of exposure to mucous membranes and medical attention was not needed. Download lagu nike ardila cinta diantara kita reggae. Material safety data sheet (msds) was not reviewed, but there is an exposure control and risk management plan in place at the facility.

The sample was collected in a microtainer collection device and was stored at room temperature for less than 30 minutes. The sample appeared normal. The instrument was performing within quality control specifications in the auto mode. The field service engineer (fse) found that the manual mode probe was bent preventing the probe wipe from completely descending all the way down the needle.

The fse installed a new blood sampling valve (bsv) to resolve the issue. The actuator valve was also replaced as a preventive measure. The fse performed a calibration adjustment to both primary and secondary mode and verified instrument operation. The cause of the leak was a bent manual mode aspirate probe. Brand Name COULTER® LH500 HEMATOLOGY ANALYZER Type of Device DIFFERENTIAL CELL COUNTER Manufacturer (Section D) BECKMAN COULTER, INC.

Kraemer blvd. Brea CA 92821 Manufacturer (Section G) BECKMAN COULTER, INC. 11800 sw 147th avenue miami FL 33196 Manufacturer Contact dung nguyen 250 s. Kraemer blvd. Brea, CA 614941 MDR Report Key 2646586 Report Number 10-02071 Device Sequence Number 1 Product Code Report Source Manufacturer Source Type Health Professional,User facility Reporter Occupation Other Type of Report Initial Report Date 1 Device Was Involved in the Event 0 PatientS WERE Involved in the Event: Date FDA Received Is This An Adverse Event Report?

No Is This A Product Problem Report? Yes Device Operator Health Professional Device MODEL Number LH500 Device Catalogue Number 178833 OTHER Device ID Number SOFTWARE V. 2A5 Was Device Available For Evaluation? Yes Is The Reporter A Health Professional? No Date Manufacturer Received Was Device Evaluated By Manufacturer? Yes Date Device Manufactured Is The Device Single Use?

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No Is this a Reprocessed and Reused Single-Use Device? No Type of Device Usage Invalid Data.