MAUDE Adverse Event Report: SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED IMMULITE 2000 IGFBP-3; RADIOIMMUNOASSAY, HUMAN GROWTH HORMONE

Model Number	N/A
Medical Device Problem Code	Low Test Results (2458)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	12/04/2025
Type of Reportable Event	Malfunction
Event or Problem Description
The customer performed a routine reset for the igfbp-3 (insulin-like growth factor binding protein 3) assay, measured on the immulite 2000 xpi analyzer #o6345, after the moving median registered in the customer's system was rejected.The moving median is used as a patient-based quality control.For every 30 patient results, the system generates a median value, which is plotted on a monitoring graph.For this assay, the median registered on the graph is 4.97, with a standard deviation (sd) of 0.27.If the moving median value exceeds the limits established by the 1x 3sd or 2x 2sd rejection rules, the customer performs an evaluation of the previous routine.In this case, the previous routine was evaluated and discrepancies in results were identified in patient samples.The patient samples were repeated on the same analyzer the following day.It is unknown whether a different reagent wedge/bead was used for the repeat testing on the same analyzer.The initial results for the discordant patient samples were reported and were not questioned by the physician(s).The laboratory did not send corrected results for these discordant patient results.There are no known reports of patient intervention or adverse health consequences due to the discordant igfbp-3 results.
Additional Manufacturer Narrative
An outside united states (ous) customer contacted a siemens customer care center to report discordant igfbp-3 results that were obtained on patient samples on an immulite 2000 xpi instrument.Quality controls (qcs) were in range at the time of the event.The adjustment in use at the time of the event was acceptable.The same adjustment was in use for both the initial and repeat results.There were no events identified in the message log for the instrument that would explain the discordant results.The moving median returned to performing within the acceptable range on 05-dec-2025.Per the limitation section of the immulite 2000 igfbp-3 instructions for use (ifu): "for diagnostic purposes, the results obtained from this assay should always be used in combination with the clinical examination, patient medical history, and other findings." siemens is investigating.
Additional Manufacturer Narrative
Siemens filed the initial mdr 1219913-2026-00007 on 07-jan-2026.Additional information 11-feb-2026: siemens healthineers reviewed the information provided.Troubleshooting was performed at customer site: samples were repeated on alternative analyzers and on the same analyzer.It was noted that the discrepancies did not occur at a specific point in time but were distributed over time.However, when the results were evaluated by concentration, a pattern of low results at low concentrations, especially around approximately 2.0 g/ml occurred.The moving median returned to performing within the acceptable range on (b)(6) 2025.The routine quality controls (qc) remained within specifications throughout the entire period.The control measurements did not show any abnormalities and are within the expected range, and the adjustment done on december 2, 2025 was successfully completed and is acceptable.A contamination in the instrument would be expected to lead to significantly more discrepant results; therefore, instrument contamination is not suspected.This indicates that there was no instrument or assay issue.Error log evaluation did not reveal specific error messages which could lead to a discordant sample result.Spy-files do not show any irregularities in pipetting or similar processes.Encoder values did not reveal any occurrences of foam or bubbles on the reagent.Delta values between the different reagent aspiration steps are as expected.The difference in successive level sense, the delta, reflects how much reagent was removed when the reagent was aspirated the previous time.No cause for the discordant patient results could be identified.The most likely cause is due pre-analytical variables, such as insufficient centrifugation of the sample.Since the samples were received frozen, insufficient centrifugation and/or other pre-analytical variables could not be ruled out.No other complaints have been received for immulite 2000 igfbp-3 kit lot 442.The immulite 2000 igfbp-3 kit lot 442 is performing as intended.A product performance issue has not been identified.No further evaluation of the device is required.In section h6, the investigation findings and investigation conclusions codes were updated.

• Brand Name: IMMULITE 2000 IGFBP-3
• Common Device Name: RADIOIMMUNOASSAY, HUMAN GROWTH HORMONE
• Manufacturer (Section D): SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED; glyn rhonwy; llanberis, gwynedd LL55 4EL; UK LL55 4EL
• Manufacturer (Section G): SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED; glyn rhonwy; uk registration #: 3002806944; llanberis, gwynedd LL55 4EL; UK LL55 4EL
• Manufacturer Contact: karen confort ; 333 coney st.; east walpole, MA 02032 ; 3392069063
• MDR Report Key: 23988654
• Report Number: 1219913-2026-00007
• Device Sequence Number: 11919907
• Product Code: CFL
• UDI-Device Identifier: 00630414966113
• UDI-Public: (01)00630414966113(10)442(17)260620
• Combination Product (Y/N): N
• Initial Reporter Country: BR
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 02/13/2026

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 Date: 06/20/2026
• Device Model Number: N/A
• Device Catalogue Number: 10381447
• Device Lot Number: 442
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/17/2025
• Supplement Date Received by Manufacturer: 02/11/2026
• Initial Report FDA Received Date: 01/07/2026
• Supplement Report FDA Received Date: 02/13/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 06/20/2025
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown