Elecsys Anti-HBc II 09014926162Recalls & reported problems
Roche Diagnostics GmbH · Class U
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613336183106), received between Dec 23, 2025 and Aug 24, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “False Negative Result” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- False Negative Result2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 24, 2026False Negative Result
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50416476 ↗MalfunctionDec 23, 2025False Negative Result; False Negative Result
THERE WAS AN ALLEGATION OF QUESTIONABLE ELECSYS ANTI-HBC II RESULTS FROM THE COBAS E 801 ANALYTICAL UNIT WHILE PERFORMING VALIDATION TESTING. THE INITIAL RESULT WAS REPEATEDLY POSITIVE USING AN ABBOT ALINITY SYSTEM. THE REPEAT RESULT FROM THE COBAS E801 WAS 2.23 COI (NON-REACTIVE). NO QUESTIONABLE RESULT WAS REPORTED OUTSIDE OF THE LABORATORY. IT WAS UNKNOWN WHICH RESULT WAS CORRECT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23876450 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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