SYNCHRON? URIC ACID REAGENT 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 2011-03-28 for SYNCHRON? URIC ACID REAGENT 442785 manufactured by Beckman Coulter, Inc..

Event Text Entries

[20734599] A synchron uric acid reagent pack was found leaking in beckman coulter warehouse. There was no exposure to uncovered wounds or mucous membranes. No injury was reported.
Patient Sequence No: 1, Text Type: D, B5


[20833712] The liquid leaked because the cap was loose. The incident occurred at bci warehouse.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2050012-2011-00885
MDR Report Key2032169
Report Source00,01
Date Received2011-03-28
Date of Report2011-02-28
Date of Event2011-02-28
Date Mfgr Received2011-02-28
Device Manufacturer Date2010-12-06
Date Added to Maude2012-02-02
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 CA 92821
Manufacturer CountryUS
Manufacturer Postal Code92821
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSYNCHRON? URIC ACID REAGENT
Generic NameURIC ACID REAGENT
Product CodeKNK
Date Received2011-03-28
Model NumberNA
Catalog Number442785
Lot NumberM012242
OperatorHEALTH PROFESSIONAL
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 2011-03-28

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