MAUDE Adverse Event Report: ORTHO-CLINICAL DIAGNOSTICS, INC. VITROS CHEMISTRY PRODUCTS CALIBRATOR KIT 2; IN-VITRO DIAGNOSTICS

Catalog Number	1662659
Medical Device Problem Code	High Test Results (2457)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/03/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The investigation determined that higher than expected vitros na+ and vitros k+ results were obtained from a single level of a non-vitros thermofisher mas control (lot: ocr2608) using vitros na+ slide lot: 4272-1152-0701 and vitros k+ slide lot: 4102-0918-6250 on a vitros xt 7600 integrated system.The assignable cause of the event is suboptimal calibrations of both the vitros na+ and k+ assays.The event started with calibration events that occurred on 03 july 2025.The calibration slope parameter appeared atypical to expected slope parameters and post calibration quality control results were unacceptable.The cause of the suboptimal calibration was improper reconstitution of the vitros calibrator kit 2 fluids.The vitros calibrator kit 2 instructions for use (ifu) states add 3.0 ml of the appropriate diluent to each vial.Use a clean, dry pipette for each vial.A class a volumetric pipette or an automated pipette of equivalent accuracy is recommended because of the importance of this reconstitution procedure to the accuracy of the results.Discard any remaining diluent.The customer admitted to taking the entire contents of the vitros calibrator kit 2 diluent (5.0 ml) and pouring it all into the corresponding lyophilate bottles, against vitros ifu instructions.Recalibration events using proper protocol resolved the issue, as post-calibration qc results were within acceptable range.Therefore, improper protocol used by the customer while preparing vitros calibrator kit 2 fluids was the cause of the suboptimal calibration event on 03 july 2025 that led to the higher than expected vitros na+ and vitros qc k+ results.
Event or Problem Description
A customer contacted the ortho clinical diagnostics (ortho) technical solution center (tsc) to report higher than expected vitros na+ and vitros k+ results were obtained from a single level of a non-vitros thermofisher mas control (lot: ocr2608) using vitros sodium (na+) slide lot: 4272-1152-0701 and vitros potassium (k+) slide lot: 4102-0918-6250 on a vitros xt 7600 integrated system.Vitros na+ slide lot: 4272-1152-0701 mas ocr2608 l1 results of 205.4, 203.3, 203.7, 203.0, 204.6, 205.2, and 203.9 mmol/l vs.The expected result of 121.1 mmol/l vitros k+ slide lot: 4102-0918-6250 mas ocr2608 l1 results of 4.56, 4.58, 4.54, 4.53, 4.51, 4.55, 4.56, 4.6, 4.57, and 4.51 mmol/l vs.The expected result of 2.65 mmol/l biased results of the magnitude and direction observed may lead to inappropriate physician action if they were to occur undetected on patient samples.The higher-than-expected results were obtained from a non-patient quality control sample; however, the investigation cannot conclude that patient sample results were not or would not be affected if the event were to recur undetected.There were no reported allegations of patient harm as a result of this event.This report corresponds to ortho clinical diagnostics inc (ortho) complaint number: (b)(4) and reportability assessment (b)(4).

• Brand Name: VITROS CHEMISTRY PRODUCTS CALIBRATOR KIT 2
• Common Device Name: IN-VITRO DIAGNOSTICS
• Manufacturer (Section D): ORTHO-CLINICAL DIAGNOSTICS, INC.; 100 indigo creek drive; rochester NY 14626
• Manufacturer (Section G): ORTHO-CLINICAL DIAGNOSTICS, INC.; 1000 lee road; rochester NY 14606
• Manufacturer Contact: laurie o'riordan ; 1295 southwest 29th avenue; pompano beach, FL 33069 ; 9549709500
• MDR Report Key: 22665150
• Report Number: 1319808-2025-00028
• Device Sequence Number: 11687868
• Product Code: JIX
• UDI-Device Identifier: 10758750009503
• UDI-Public: (01)10758750009503(17)260701(11)240701(10)0214
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Health Professional
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 07/30/2025

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 Expiration Date: 07/01/2026
• Device Catalogue Number: 1662659
• Device Lot Number: 0214
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/17/2025
• Initial Report FDA Received Date: 07/30/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 07/01/2024
• 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
• Patient Sex: Unknown