DCA 2000+

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2013-01-07 for DCA 2000+ manufactured by Siemens Healthcare Diagnostics.

Event Text Entries

[21988217] Customer has reported 3 examples of albumin/creatinine ratio (acr) results which have not correlated with the pts acr trend. No injury was reported with the event.
Patient Sequence No: 1, Text Type: D, B5


[22201776] Customer reported 3 examples of albumin/creatinine ratio (acr) results which have not correlated with the pts acr trend. The customer sent the samples for confirmation testing to another laboratory to confirm the results were incorrect. The(b)(4) who oversee this customer are concerned that the albumin results did not flag appropriately at >300 mg/l. (pt 3 did report correctly) however, sample 2 should have, given the package insert indicates up to 2000 mg/l. Mfr is investigating.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1217157-2012-00064
MDR Report Key2913603
Report Source07
Date Received2013-01-07
Date of Report2012-11-08
Date of Event2012-11-08
Date Mfgr Received2012-11-08
Date Added to Maude2013-02-01
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 ContactMARK SMITH
Manufacturer Street2 EDGEWATER DRIVE
Manufacturer CityNORWOOD MA 02062
Manufacturer CountryUS
Manufacturer Postal02062
Manufacturer Phone7812693158
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS MANUFACTURING, LTD.
Manufacturer StreetNORTHERN ROAD
Manufacturer CitySUDBURY, SUFFOLK CO102XQ
Manufacturer CountryUK
Manufacturer Postal CodeCO10 2XQ
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDCA 2000+
Generic NameDCA 2000+
Product CodeJIR
Date Received2013-01-07
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS
Manufacturer Address511 BENEDICT AVENUE TARRYTOWN NY 10591 US 10591


Patients

Patient NumberTreatmentOutcomeDate
10 2013-01-07

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.