Liquichek 596Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00847661001201), received between Mar 25, 2025 and Mar 25, 2025 — classified as 1 malfunction.

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. How this data works · Data updated Oct 13, 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.

• MalfunctionMar 25, 2025No Apparent Adverse Event; No Apparent Adverse Event

  ON (B)(6) 2025, A LABORATORY TECHNICIAN AT (B)(6), LOCATED AT (B)(6), REPORTED AN EYE SPLASH INCIDENT INVOLVING THEMSELVES. THE TECHNICIAN WAS NOT WEARING SAFETY GLASSES WHILE DISCARDING A QC SAMPLE CUP INTO A NEARLY FULL BIOHAZARD BIN. WHEN THE CUP, CONTAINING THE LIQUICHEK IMMUNOLOGY CONTROL QC SAMPLE, BOUNCED BACK AFTER BEING TOSSED, LIQUID SPRAYED INTO THE TECHNICIAN'S LEFT EYE. THE TECHNICIAN IMMEDIATELY RINSED THEIR EYE AT THE EYE WASH STATION. AFTERWARD, THEY CONTACTED THE HOSPITAL AND WERE PRESCRIBED ANTIVIRAL EYE DROPS OVER THE PHONE. NO HARM OR INJURY RESULTED FROM THIS EVENT. THE EMPLOYEE AND FACILITY HAD PRODUCT'S INSTRUCTIONS FOR USE (IFU) AND SAFETY DATA SHEET (SDS) AND WERE PROVIDED INSTRUCTIONS OVER THE PHONE OF HOW TO OBTAIN THE CERTIFICATE OF ANALYSIS.

  Patient problems: Unspecified Eye / Vision Problem

  MAUDE report 21691818 ↗