ACCESS? IMMUNOASSAY SYSTEM R81600

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 2010-04-02 for ACCESS? IMMUNOASSAY SYSTEM R81600 manufactured by Beckman Coulter Inc..

Event Text Entries

[1301180] A customer obtained lower than expected results for progesterone on two (2) patients' samples. A) the results were reported out of the lab. B) one patient was treated with progesterone and subsequent testing still resulted low. C) the second patient's sample was tested on an alternate method and recovered higher results that fit the patient's clinical picture.
Patient Sequence No: 1, Text Type: D, B5


[8589777] Sample collection and system performance information was not supplied. Service was not dispatched for this event. A malfunction will be assumed for the purpose of this report.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2122870-2010-00120
MDR Report Key1649346
Report Source05
Date Received2010-04-02
Date of Report2010-04-02
Date of Event2010-02-25
Date Mfgr Received2010-03-04
Device Manufacturer Date2000-03-17
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 Professional3
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
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameACCESS? IMMUNOASSAY SYSTEM
Generic NameDISCRETE PHOTOMETRIC CHEMISTRY ANALYZER
Product CodeMXZ
Date Received2010-04-02
Model NumberACCESS? IMMUNOASSAY SYSTEM
Catalog NumberR81600
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 2010-04-02

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