Liquichek 27104Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00847661004172), received between Feb 24, 2020 and Feb 24, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Human-Device Interface Problem” (1 report).

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 16, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 24, 2020Human-Device Interface Problem; Human-Device Interface Problem

  ON (B)(6) 2020, A MEDICAL TECHNOLOGIST FROM (B)(6) LAB CALLED BIO-RAD QSD TECHNICAL SUPPORT TO REPORT A POTENTIAL ADVERSE EVENT THAT OCCURRED WITH AN EMPLOYEE AT THEIR FACILITY. THE EMPLOYEE WAS OPENING A VIAL OF LIQUICHEK CARDIAC MARKERS PLUS CONTROL LT, LEVEL 1A, LOT # 23694 AND THE CONTENTS SPLASHED ONTO HER RIGHT EYE WHILE NOT WEARING SAFETY GOGGLES. THE EMPLOYEE WASHED AND FLUSHED HER EYES AND ALSO WASHED HER FACE. THE INCIDENT WAS REPORTED TO FACILITIES HEALTH AND THE EMPLOYEE WAS SEEN BY A DOCTOR. NO MEDICAL TESTS WERE DONE. THE EMPLOYEE HAD ALL THE SCREENINGS DONE AT PRE-EMPLOYMENT TIME. THE EMPLOYEE AND FACILITY HAVE ACCESS TO PRODUCT'S PACKAGE INSERT, MSDS AND COA.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9745217 ↗