MAUDE Adverse Event Report: ROCHE DIAGNOSTICS ELECSYS HBEAG; TEST, HEPATITIS B (B CORE, BE ANTIGEN, BE ANTIBODY, B CORE IGM)

Catalog Number	07027427190
Medical Device Problem Code	False Positive Result (1227)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/07/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Complete e1 initial reporter street address: (b)(6).Qc and calibration data did not show any abnormalities.The patient sample has been requested for investigation.The investigation is ongoing.
Event or Problem Description
There was an allegation of a questionable elecsys hbeag result from the cobas e 801 analytical unit for one patient.The affected patient also had questionable elecsys hbsag ii and elecsys® anti-hbc ii results.This medwatch will apply to the elecsys hbeag assay.Please refer to the medwatch with a1.Patient identifier: (b)(6) for the elecsys hbsag ii assay and medwatch with a1.Patient identifier: (b)(6)2 for the elecsys® anti-hbc ii assay.

• Brand Name: ELECSYS HBEAG
• Common Device Name: TEST, HEPATITIS B (B CORE, BE ANTIGEN, BE ANTIBODY, B CORE IGM)
• 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: 24832994
• Report Number: 1823260-2026-01363
• Device Sequence Number: 9169057
• Product Code: LOM
• UDI-Device Identifier: 04015630939862
• UDI-Public: 04015630939862
• Combination Product (Y/N): N
• Initial Reporter Country: CH
• PMA/510(K) Number: P130015/S017
• 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,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 06/18/2026

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 Catalogue Number: 07027427190
• Device Lot Number: 847419
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 03/16/2026
• Supplement Date Received by Manufacturer: 05/21/2026
• Initial Report FDA Received Date: 04/09/2026
• Supplement Report FDA Received Date: 06/18/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• 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