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Liquichek 751Recalls & reported problems

Bio-Rad Laboratories, Inc. · Liquichek Spinal Fluid Control Level 1 (A human based assayed spinal fluid 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 00847661001584), received between Oct 24, 2017 and Oct 24, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Human Factors Issue” (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 Factors Issue1

Patient problems

  • Alteration In Body Temperature1
  • Rash1

Recent adverse event reports

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

  • MalfunctionOct 24, 2017Human Factors Issue; Human Factors Issue

    ON OCTOBER 10, 2017 BIO-RAD (B)(4) RECEIVED A REPORT FROM THE UNIVERSITY (B)(6) IN THE (B)(6) OF AN EYE SPLASH INVOLVING LIQUICHEK SPINAL FLUID CONTROL THAT HAD OCCURRED APPROXIMATELY 4 WEEKS EARLIER. A LAB TECHNICIAN HAD SPLASHED THE SPINAL FLUID CONTROL INTO HER EYE. SHE HAD RECENTLY DEVELOPED A "RASH AND TEMPERATURE RISE CONSISTENT WITH (B)(6)".

    Patient problems: Alteration In Body Temperature; Rash

    MAUDE report 6974280 ↗

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.