SYNCHRON URIC ACID 442785

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,01 report with the FDA on 2011-06-10 for SYNCHRON URIC ACID 442785 manufactured by Beckman Coulter Inc..

Event Text Entries

[19709577] No additional information was provided. Cx/lx iron ferrous kit, catalog number : 467910, lot number: m008562, classification code jiy, 510k: k960485, date of manufacture: 10/12/2010. Cx/lx valproic acid, catalog number : 467995, lot number: m102369, classification code leg, 510k: k961256, date of manufacture: 01/31/2011.
Patient Sequence No: 1, Text Type: N, H10


[19844246] Beckman coulter inc. (bci) (b)(4) reported cx uric acid reagent, cx/lx iron ferrous, cx/lx valproic acid cartridges leaked and were unable to determine to source of the leak. No injury was reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2050012-2011-02258
MDR Report Key2120810
Report Source00,01
Date Received2011-06-10
Date of Report2011-05-12
Date of Event2011-05-12
Date Mfgr Received2011-05-12
Device Manufacturer Date2011-03-29
Date Added to Maude2012-02-21
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 KRAEMER BLVD.
Manufacturer CityBREA CA 92821
Manufacturer CountryUS
Manufacturer Postal92821
Manufacturer Phone7149613634
Manufacturer G1BECKMAN COULTER INC.
Manufacturer Street250 S. KRAEMER BLVD
Manufacturer CityBREA CA 92821
Manufacturer CountryUS
Manufacturer Postal Code92821
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSYNCHRON URIC ACID
Generic NameCX URIC ACID REAGENT
Product CodeKNK
Date Received2011-06-10
Model NumberURIC ACID
Catalog Number442785
Lot NumberM103154
ID NumberN/A
OperatorOTHER
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerBECKMAN COULTER INC.
Manufacturer Address250 S. KRAEMER BLVD BREA CA 92821 US 92821


Patients

Patient NumberTreatmentOutcomeDate
10 2011-06-10

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