UNICEL? DXI 800 ACCESS? IMMUNOASSAY SYSTEM 973100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2010-03-15 for UNICEL? DXI 800 ACCESS? IMMUNOASSAY SYSTEM 973100 manufactured by Beckman Coulter Inc..

Event Text Entries

[1484611] A customer obtained erroneously low progesterone results on one patient. The tech questioned the results and ran the sample on a different instrument which gave a result of 0. 71ng/ml. The result was reported out of the lab. Customer then recalibrated progesterone assay on the dxi 800 analyzer. Progesterone testing was repeated, and a result of 0. 49ng/ml was obtained. The erroneous results were not reported out of the lab. The customer did not report affect to the patient or user attributed or connected to this event.
Patient Sequence No: 1, Text Type: D, B5


[8447738] The specimen was collected in a red top corvac tube with gel, and was sampled from the primary tube. Qc was within specifications prior to the event. A field service engineer (fse) was dispatched: the fse performed a diagnostic testing which met specifications. A definitive root cause for this event has not been determined to date. A malfunction will be assumed for the purpose of this report.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2122870-2010-00094
MDR Report Key1630872
Report Source05
Date Received2010-03-15
Date of Report2010-03-15
Date of Event2010-02-16
Date Mfgr Received2010-02-22
Device Manufacturer Date2006-06-19
Date Added to Maude2010-08-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMS. NORA ZEROUNIAN
Manufacturer Street250 S KRAEMER BLVD.
Manufacturer CityBREA CA 92821
Manufacturer CountryUS
Manufacturer Postal92821
Manufacturer Phone7149613634
Manufacturer G1BECKMAN COULTER INC.
Manufacturer Street1000 LAKE HAZELTINE DRIVE
Manufacturer CityCHASKA MN 55318
Manufacturer CountryUS
Manufacturer Postal Code55318
Single Use3
Remedial ActionIN
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNICEL? DXI 800 ACCESS? IMMUNOASSAY SYSTEM
Generic NameDISCRETE PHOTOMETRIC CHEMISTRY ANALYZER
Product CodeMXZ
Date Received2010-03-15
Model NumberNA
Catalog Number973100
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerBECKMAN COULTER INC.
Manufacturer Address1000 LAKE HAZELTINE DRIVE CHASKA MN 55318 US 55318


Patients

Patient NumberTreatmentOutcomeDate
10 2010-03-15

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.