MAUDE Adverse Event Report: ABBOTT LABORATORIES ARCHITECT C4000 PROCESSING MODULE; ANALYZER, CHEMISTRY (PHOTOMETRIC, DISCRETE), FOR CLINICAL USE

Catalog Number	02P24-01
Medical Device Problem Code	High Test Results (2457)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/03/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
This issue was previously reported under mdr number 3005094123-2025-00399 under a different suspect device.Complete entry for section a1 - patient identifier: (b)(6).An evaluation is in process.A follow-up report will be submitted when the evaluation is complete.All available patient information was included.Additional patient details are not available.
Event or Problem Description
The customer observed falsely elevated magnesium on the architect c4000 processing module for two patients.The following results were provided (reference range 1.5 ¿ 2.2 mg/dl): on (b)(6) 2025, sid (b)(6) (newborn), initial magnesium result= 5.95 mg/dl; (b)(6) 2025, repeat result= 2.10 mg/dl.(b)(6) 2025, sid (b)(6), initial magnesium result= 8.54 mg/dl; repeat result= 1.70 mg/dl.There was no impact to patient management reported.
Additional Manufacturer Narrative
The field service representative (fsr) inspected the architect c4000 processing module, serial number (b)(6), cleaned the cuvettes and replaced the cc cuv dry tip.The replacement of the cc cuv dry tip resolved the issue.An instrument service history review of the architect c4000 revealed no additional issues of false elevated patient results reported on the (b)(6).A review of tracking and trending of the architect c4000 did not identify an increase in complaint activity associated with the complaint issue.A review of tracking and trending for the cc cuv dry tip did not identify an increase in complaint activity.A review of the manufacturing documentation did not identify any issues associated with the complaint issue.Labeling was reviewed and found to be adequate.Based on the available information, no systemic issue or deficiency of the architect i4000 processing module for serial number (b)(6) or the cc cuv dry tip was identified.
Event or Problem Description
The customer observed falsely elevated magnesium on the architect c4000 processing module for two patients.The following results were provided (reference range 1.5 ¿ 2.2 mg/dl): (b)(6) 2025, sid (b)(6) (newborn), initial magnesium result= 5.95 mg/dl; (b)(6) 2025, repeat result= 2.10 mg/dl.(b)(6) 2025, sid (b)(6), initial magnesium result= 8.54 mg/dl; repeat result= 1.70 mg/dl.There was no impact to patient management reported.

• Brand Name: ARCHITECT C4000 PROCESSING MODULE
• Common Device Name: ANALYZER, CHEMISTRY (PHOTOMETRIC, DISCRETE), FOR CLINICAL USE
• Manufacturer (Section D): ABBOTT LABORATORIES; 1915 hurd drive; irving TX 75038
• Manufacturer (Section G): ABBOTT LABORATORIES; 1915 hurd drive; irving TX 75038
• Manufacturer Contact: nicole jenne ; max-planck-ring 2; post market surveillance; wiesbaden 65205 ; GM 65205 ; 6122582960
• MDR Report Key: 22955968
• Report Number: 3016438761-2025-00505
• Device Sequence Number: 8404612
• Product Code: JJE
• UDI-Device Identifier: 00380740003746
• UDI-Public: (01)00380740003746
• Combination Product (Y/N): N
• Initial Reporter Country: BR
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 09/05/2025

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 Catalogue Number: 02P24-01
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/20/2025
• Supplement Date Received by Manufacturer: 09/04/2025
• Initial Report FDA Received Date: 09/03/2025
• Supplement Report FDA Received Date: 09/05/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 07/03/2012
• 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
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: CC CUV DRY TIP, 09D51-02, UNKNOWN.; CC MAGNESIUM (1000T), 03P68-24, 71414UD00.; CC MAGNESIUM (1000T), 03P68-24, 71414UD00.
• Patient Sex: Unknown