MAUDE Adverse Event Report: ROCHE DIAGNOSTICS ELECSYS T3; TOTAL TRIIODOTHYRONINE TEST

Model Number	T3
Medical Device Problem Code	Incorrect, Inadequate or Imprecise Result or Readings (1535)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Event or Problem Description
1.There was an allegation of questionable elecsys t3 results for one patient from the cobas 6000 e601 module.2.Patient age range: 53 years.3.Patient weight range: asku.4.Patient sex breakdown: male.5.Patient race breakdown: asku.6.Patient ethnicity breakdown: asku.
Additional Manufacturer Narrative
1.Summary of investigation results: sample material from the patient was requested for further investigation.2.Summary of follow up/corrective actions taken: investigation is ongoing.3.Device returned to manufacturer? no.4.Device labeled "for single use?" no.5.Device reprocessed and reused? no.
Additional Manufacturer Narrative
1.Summary of investigation results: sample material from the patient was tested, and no interfering factors were detected.There was no evidence of a device malfunction.2.Summary of follow up/corrective actions taken: none.

• Brand Name: ELECSYS T3
• Common Device Name: TOTAL TRIIODOTHYRONINE TEST
• Manufacturer (Section D): ROCHE DIAGNOSTICS; 9115 hague road; indianapolis IN 46250 0457
• Manufacturer (Section G): ROCHE DIAGNOSTICS GMBH; sandhofer strasse 116; mannheim (baden-wurttemberg) 68305 ; GM 68305
• Manufacturer Contact: natalie catton ; 9115 hague road; indianapolis, IN 46250
• MDR Report Key: 23369194
• Report Number: 1823260-2025-04312
• Device Sequence Number: 15935537
• Product Code: CDP
• UDI-Device Identifier: 07613336171646
• UDI-Public: 07613336171646
• Combination Product (Y/N): N
• PMA/510(K) Number: EXEMPT
• Exemption Number: VMSR
• Number of Events Summarized: 1
• Summary Report (Y/N): Y
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 04/27/2026

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?: No
• Device Model Number: T3
• Device Catalogue Number: 09007725190
• Device Lot Number: ASKU
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: Not provided
• Supplement Date Received by Manufacturer: 02/23/2026
• Initial Report FDA Received Date: 10/23/2025
• Supplement Report FDA Received Date: 04/27/2026
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown