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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW DIMENSION VISTA®; DIMENSION VISTA® FT4 FREE THYROXINE FLEX® REAGENT CARTRIDGE

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SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW DIMENSION VISTA®; DIMENSION VISTA® FT4 FREE THYROXINE FLEX® REAGENT CARTRIDGE Back to Search Results
Catalog Number K6410 SMN 10445103
Medical Device Problem Code High Test Results (2457)
Health Effect - Clinical Code No Known Impact Or Consequence To Patient (2692)
Date of Event 06/06/2017
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
The customer contacted siemens healthcare diagnostics concerning the impact of biotin on the ft4 result on a patient that had been receiving a dosage of quizenday biotin.The questioned result was obtained after dosage was stopped.The cause for the discordant elevated ft4 result is unknown.Siemens is investigating the incident.
 
Event or Problem Description
A discordant elevated free thyroxine (ft4) result was obtained on a patient sample on the dimension vista 500 system.The result was not reported to the physician.The result was questioned within the laboratory.There are no reports of patient intervention or adverse health consequences as a result of the discordant elevated ft4 result.
 
Additional Manufacturer Narrative
The original mdr was filed 6/29/2017.The ft4 assay has been tested for potential interference at biotin levels of 100, 250, 500, and 1200 ng/ml.Interference testing was performed following clinical laboratory standards institute (clsi) guidance at concentrations approximately equivalent to the levels listed in the ifu.Below is the biotin interference of dimension vista ft4: test level: 1.4, units: ng/dl, biotin test level and % interference observed, 1200 ng/ml, 500 ng/ml 37.6%, 250 ng/ml 8.4%, 100 ng/ml 1.5%, result for sample with 1200 ng/ml biotin is above the analytical measurement range and percentage increase could not be calculated.The siemens investigation is continuing.
 
Additional Manufacturer Narrative
Siemens healthcare diagnostics concluded the investigation of potential interference of biotin on dimension vista ft4 results.The instructions for use for the dimension vista ft4 flex reagent cartridge has been revised to include in the limitations of procedure section the following statement: "specimens that contain biotin at a concentration of 100 ng/ml demonstrate a less than or equal to 10% change in results.Biotin concentrations greater than this may lead to falsely elevated results for patient samples.Results from patients taking biotin supplements or receiving high-dose biotin therapy should be interpreted with caution due to possible interference with this test.".
 
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Brand Name
DIMENSION VISTA®
Common Device Name
DIMENSION VISTA® FT4 FREE THYROXINE FLEX® REAGENT CARTRIDGE
Manufacturer (Section D)
SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW
glasgow business community
500 gbc drive po box 6101
newark DE 19714 6101
MDR Report Key6678894
Report Number2517506-2017-00559
Device Sequence Number72800
Product Code CEC
UDI-Device Identifier00842768015205
UDI-Public00842768015205
Combination Product (Y/N)N
Initial Reporter CountryFR
PMA/510(K) Number
K140859
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source foreign,health professional,u
Initial Reporter Occupation Health Professional
Type of Report Initial,Followup,Followup
Report Date (Section B) 01/26/2018
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Expiration Date01/12/2018
Device Catalogue NumberK6410 SMN 10445103
Device Lot Number17012BA
Was Device Available for Evaluation? No
Was the Report Sent to FDA? No
Initial Date Received by Manufacturer 06/09/2017
Supplement Date Received by Manufacturer07/28/2017
01/04/2018
Initial Report FDA Received Date06/29/2017
Supplement Report FDA Received Date08/24/2017
01/26/2018
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
Patient Age41 YR
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