SYNCHRON CX3 DELTA 467501

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2011-02-06 for SYNCHRON CX3 DELTA 467501 manufactured by Beckman Coulter Inc..

Event Text Entries

[1815983] A customer contacted beckman coulter inc. , (bci) and stated that creatinine reagent is leaking from back of synchron cx3 delta instrument onto floor, and was unable to locate the source of the leak. No patient results were generated in this event. No injury was reported on this issue.
Patient Sequence No: 1, Text Type: D, B5


[8844231] A field service engineer (fse) was dispatched: the fse found waste line came loose from bulkhead inside of instrument. The fse reconnected tubing onto bulkhead and primed to verify draining properly. The fse cleaned the spill.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2050012-2011-00350
MDR Report Key1979665
Report Source07
Date Received2011-02-06
Date of Report2011-01-12
Date of Event2011-01-12
Date Mfgr Received2011-01-12
Device Manufacturer Date1995-10-21
Date Added to Maude2012-01-25
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 Street250 S. KRAEMER BLVD.
Manufacturer CityBREA 92821
Manufacturer CountryUS
Manufacturer Postal Code92821
Single Use3
Remedial ActionRP
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSYNCHRON CX3 DELTA
Generic NameCLINICAL CHEMISTRY ANALYZER
Product CodeJJF
Date Received2011-02-06
Model NumberCX3 DELTA
Catalog Number467501
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBECKMAN COULTER INC.
Manufacturer Address250 S KRAEMER BLVD. BREA CA 92821 US 92821


Patients

Patient NumberTreatmentOutcomeDate
10 2011-02-06

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