SYNCHRON? CK N/A 476836

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2011-04-22 for SYNCHRON? CK N/A 476836 manufactured by Beckman Coulter Inc..

Event Text Entries

[18178671] A customer contacted beckman coulter inc. (bci) to report receiving a leaking synchron ck reagent. No injury was reported for this event.
Patient Sequence No: 1, Text Type: D, B5


[18203446] A replacement was sent to the customer.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2050012-2011-01244
MDR Report Key2067470
Report Source06
Date Received2011-04-22
Date of Report2011-03-24
Date of Event2011-03-24
Date Mfgr Received2011-03-24
Device Manufacturer Date2010-12-14
Date Added to Maude2012-02-06
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
Remedial ActionRL
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameSYNCHRON? CK
Generic NameSYNCHRON? CK
Product CodeCKA
Date Received2011-04-22
Model NumberN/A
Catalog Number476836
Lot NumberM010495
Device Expiration Date2011-07-31
Device AvailabilityN
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 2011-04-22

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