MAUDE Adverse Event Report: SIEMENS HEALTHCARE DIAGNOSTICS INC. DIMENSION ENZYMATIC CARBONATE FLEX REAGENT CARTRIDGE; ENZYMATIC, CARBON-DIOXIDE

Model Number	N/A
Medical Device Problem Code	High Test Results (2457)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/26/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The customer reported to siemens they obtained erroneously elevated enzymatic carbonate (eco2) results on six (6) patient samples on a dimension exl 200 integrated chemistry system.The erroneously elevated results were not reported to the physician(s).The same samples were reprocessed on the same dimension exl 200 integrated chemistry system.Lower results were obtained, considered correct and reported to the physician(s).There are no known reports of patient intervention or adverse health consequences due to the erroneously elevated eco2 results.
Additional Manufacturer Narrative
A united states (us) customer contacted the siemens healthcare diagnostics remote services center (rsc) regarding erroneously elevated enzymatic carbonate (eco2) results on six (6) patient samples on a dimension exl 200 integrated chemistry system.Customer stated prior to the patient samples being run, millipore water system maintenance was performed.Siemens recommended the following actions: dump/rinse the water bottle, use a new well on eco2 flex and rerun quality control (qc) and patient samples.Customer stated that after the recommended troubleshooting, the qc is within the laboratory range, and the patient samples were reprocessed and were not elevated.Siemens healthcare diagnostics is investigating the event.
Additional Manufacturer Narrative
Additional information (06-mar-2026): siemens healthcare diagnostics service operations support (sos) concluded the investigation of the event.Sos reviewed the information provided and the troubleshooting performed (replacing the well and refreshing the water bottle).Based on the available information, the probable cause of the event is suspected to be water contamination or carryover introduced during or after the millipore water system maintenance.A potential product issue was not identified.The customer is operational.The device is performing within specifications.No further evaluation is required.In section h6, the investigation finding and investigation conclusion codes were updated.Initial mdr 2517506-2026-00047 was filed on 04-mar-2026.

• Brand Name: DIMENSION ENZYMATIC CARBONATE FLEX REAGENT CARTRIDGE
• Common Device Name: ENZYMATIC, CARBON-DIOXIDE
• Manufacturer (Section D): SIEMENS HEALTHCARE DIAGNOSTICS INC.; 500 gbc drive; po box 6101; newark DE 19714 6101
• Manufacturer (Section G): SIEMENS HEALTHCARE DIAGNOSTICS INC.; 500 gbc drive; po box 6101; newark DE 19714 6101
• Manufacturer Contact: eiman sulieman ; 500 gbc drive; po box 6101; newark, DE 19714-6101 ; 7372808688
• MDR Report Key: 24508255
• Report Number: 2517506-2026-00047
• Device Sequence Number: 13366103
• Product Code: KHS
• UDI-Device Identifier: 00842768005374
• UDI-Public: (01)00842768005374(10)BA6148(17)260528
• Combination Product (Y/N): N
• Initial Reporter State: KS
• Initial Reporter Country: US
• PMA/510(K) Number: K010206
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 03/10/2026

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: 05/28/2026
• Device Model Number: N/A
• Device Catalogue Number: 10444972
• Device Lot Number: BA6148
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 02/26/2026
• Supplement Date Received by Manufacturer: 03/06/2026
• Initial Report FDA Received Date: 03/04/2026
• Supplement Report FDA Received Date: 03/10/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 06/05/2025
• 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