SYNCHRON? CONTROL MULTI-LEVEL 6X20M 657365

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 2011-01-04 for SYNCHRON? CONTROL MULTI-LEVEL 6X20M 657365 manufactured by Beckman Coulter Inc..

Event Text Entries

[1723104] It was discovered in the beckman coulter inc. (bci) warehouse that the synchron control multi-level 6x20m leaked. No injury was reported.
Patient Sequence No: 1, Text Type: D, B5


[8867179] No additional information is available for this event.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2050012-2011-00050
MDR Report Key1947313
Report Source05
Date Received2011-01-04
Date of Report2010-12-07
Date of Event2010-12-07
Date Mfgr Received2010-12-07
Device Manufacturer Date2010-06-03
Date Added to Maude2011-05-04
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 BOULEVARD
Manufacturer CityBREA CA 92821
Manufacturer CountryUS
Manufacturer Postal92821
Manufacturer Phone7149613634
Manufacturer G1BECKMAN COULTER INC.
Manufacturer Street250 S. KRAEMER BOULEVARD
Manufacturer CityBREA CA 92821
Manufacturer CountryUS
Manufacturer Postal Code92821
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameSYNCHRON? CONTROL MULTI-LEVEL 6X20M
Generic NameCONTROL MULTI-LEVEL
Product CodeCKA
Date Received2011-01-04
Model NumberNA
Catalog Number657365
Lot NumberM909750
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerBECKMAN COULTER INC.
Manufacturer Address250 S. KRAEMER BOULEVARD BREA CA 92821 US 92821


Patients

Patient NumberTreatmentOutcomeDate
10 2011-01-04

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