ADVIA CENTAUR CORTISOL (COR) ASSAY N/A 04610138

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2012-05-04 for ADVIA CENTAUR CORTISOL (COR) ASSAY N/A 04610138 manufactured by Siemens Healthcare Diagnostics, Inc..

Event Text Entries

[2753505] The customer reported that they did not receive a advia centaur cortisol urgent field safety notice ((b)(4)) that was distributed to customers in march 2012. There was no report of adverse health consequences.
Patient Sequence No: 1, Text Type: D, B5


[9806679] Urgent field safety notice ((b)(4)) was provided and the information within was reviewed with the customer for understanding.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1219913-2012-00170
MDR Report Key2559373
Report Source05,06
Date Received2012-05-04
Date of Report2012-04-05
Date of Event2012-03-07
Date Mfgr Received2012-04-05
Date Added to Maude2012-09-18
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMR. STEPHEN PERRY
Manufacturer Street333 CONEY ST.
Manufacturer CityEAST WALPOLE MA 02032
Manufacturer CountryUS
Manufacturer Postal02032
Manufacturer Phone5086604163
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS, INC.
Manufacturer Street333 CONEY STREET
Manufacturer CityEAST WALPOLE MA 02032
Manufacturer CountryUS
Manufacturer Postal Code02032
Single Use3
Remedial ActionNO
Previous Use Code3
Removal Correction NumberZ-1390-2012
Event Type3
Type of Report3

Device Details

Brand NameADVIA CENTAUR CORTISOL (COR) ASSAY
Generic NameCORTISOL IMMUNOASSAY
Product CodeJFT
Date Received2012-05-04
Model NumberN/A
Catalog Number04610138
Lot Number257
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS, INC.
Manufacturer AddressTARRYTOWN NY 10591 US 10591


Patients

Patient NumberTreatmentOutcomeDate
10 2012-05-04

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