DIMENSION? CLINICAL CHEMISTRY SYSTEM RD701

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 2014-08-05 for DIMENSION? CLINICAL CHEMISTRY SYSTEM RD701 manufactured by Siemens Healthcare Diagnostics Inc - Glasgow.

Event Text Entries

[16849867] Falsely elevated n-terminal pro-brain natriuretic peptide (pbnp) results were obtained on qc samples with chemistry wash lot rd41041 on the dimension instrument. No patient results were reported to physicians. Qc results returned to within laboratory ranges with an alternate lot of chemistry wash on the instrument. Patient treatment was not altered or prescribed on the basis of the falsely elevated pbnp qc results. There was no report of adverse health consequences as a result of the falsely elevated pbnp qc results.
Patient Sequence No: 1, Text Type: D, B5


[17081553] Siemens has confirmed bacterial contamination in chemistry wash lot rd41041. A positive bias will be observed on ctni, ltni, tsh, pbnp and lpbn and a negative bias will be seen on ft4 when this lot is first placed on the instrument without recalibration of methods. Recalibration of these assays when using this lot will not correct the problem and may cause falsely high or low results. Siemens issued an urgent medical device recall dated july 2014, communication # (b)(4), to all accounts who had received the impacted lot. Customers were advised of the immediate remedial actions to be taken by the customer: immediately discontinue use and discard all inventory of chemistry wash lot rd41041. - if this lot was never in use on the instrument, no further action is needed. - if this lot had been in use: place an alternate lot of chemistry wash on the dimension system. Prime the new bottle of chemistry wash 30 times. Recalibrate the ctni, ltni, tsh, ft4, pbnp and/or lpbn assays using the alternate lot of chemistry wash onboard. For the listed assays, process quality control every 8 hours. In the urgent medical device recall communication it was stated that siemens was shipping replacement product at no charge for all orders filled with lot rd41041. As an additional precaution, a siemens customer service engineer would be making a visit to decontaminate the system(s) of customers who have used lot rd41041.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2517506-2014-00119
MDR Report Key3979561
Report Source05,06
Date Received2014-08-05
Date of Report2014-07-15
Date of Event2014-07-11
Date Mfgr Received2014-07-15
Device Manufacturer Date2014-04-13
Date Added to Maude2014-08-14
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationMEDICAL TECHNOLOGIST
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactJAMES MORGERA
Manufacturer StreetGLASGOW BUSINESS COMMUNITY PO BOX 6101
Manufacturer CityNEWARK DE 197146101
Manufacturer CountryUS
Manufacturer Postal197146101
Manufacturer Phone3026318356
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW
Manufacturer StreetGLASGOW BUSINESS COMMUNITY 500 GBC DRIVE
Manufacturer CityNEWARK DE 19714
Manufacturer CountryUS
Manufacturer Postal Code19714
Single Use3
Remedial ActionRC
Previous Use Code3
Removal Correction Number2517506-07/15/2014-003-C
Event Type3
Type of Report3

Device Details

Brand NameDIMENSION? CLINICAL CHEMISTRY SYSTEM
Generic NameCHEMISTRY WASH
Product CodeJMG
Date Received2014-08-05
Catalog NumberRD701
Lot NumberRD41041
Device Expiration Date2014-10-13
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW
Manufacturer AddressGLASGOW BUSINESS COMMUNITY 500 GBC DRIVE NEWARK DE 19714 US 19714


Patients

Patient NumberTreatmentOutcomeDate
10 2014-08-05

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