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Liquichek 642Recalls & reported problems

Bio-Rad Laboratories, Inc. · Liquichek Lipids Control Level 2 (A human serum assayed lipids control.) · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00847661001256), received between Sep 21, 2018 and Sep 21, 2018 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Human-Device Interface Problem1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionSep 21, 2018Human-Device Interface Problem; Human-Device Interface Problem

    ON (B)(6) A PHYSICIAN ASSISTANT CALLED TO REPORT THAT SHE HAD A PATIENT SEEKING TREATMENT. THE PATIENT SPLASHED LIQUICHEK LIPIDS CONTROL, LOT 57542, INTO HER RIGHT EYE AND ON HER LEFT CHEEK. THE USER WAS NOT WEARING LABORATORY GOGGLES BUT WAS WEARING REGULAR EYEGLASSES. PHYSICIAN ASSISTANT IRRIGATED HER EYE WITH SALINE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7899083 ↗

Other Multi-analyte controls, all kinds (assayed) devices

All Multi-analyte controls, all kinds (assayed) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.