Liquichek 547Recalls & reported problems
Bio-Rad Laboratories, Inc. · Liquichek Tumor Marker Control Level 1 (A human based assayed tumor marker control.) · Class 1
All models of Liquichek (21)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00847661001447), received between Nov 20, 2018 and Nov 20, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.
MalfunctionNov 20, 2018Human-Device Interface Problem; Human-Device Interface Problem
ON (B)(6) 2018, BIO-RAD QSD TECHNICAL SUPPORT RECEIVED A CALL FROM BIO-RAD (B)(4) REPORTING A POTENTIAL ADVERSE EVENT. DR. (B)(6) AT HOSPITAL (B)(6) REPORTED THAT MRS. (B)(6), A LABORATORY TECHNICIAN DROPPED LIQUICHEK TUMOR MARKER CONTROL LOT #23951 ON THE FLOOR AND IT SPLASHED INTO HER EYE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8089923 ↗
Other Multi-analyte controls, all kinds (assayed) devices
- MAS Omni-CARDIO Liquid Assayed Integrated Cardiac Control OCRD-202Microgenics Corporation · Multi-Analyte Controls, All Kinds (Assayed)1 recall0 reports
- MAS Omni-CARDIO Liquid Assayed Integrated Cardiac Control OCRD-LMicrogenics Corporation · Multi-Analyte Controls, All Kinds (Assayed)1 recall0 reports
- MAS Omni-CARDIO Liquid Assayed Integrated Cardiac Control OCRD-101Microgenics Corporation · Multi-Analyte Controls, All Kinds (Assayed)1 recall0 reports
- Cholestech LDX™ 88773Alere San Diego, Inc. · Multi-Analyte Controls, All Kinds (Assayed)1 recall0 reports
- MAS Omni-CARDIO Liquid Assayed Integrated Cardiac Control OCRD-303Microgenics Corporation · Multi-Analyte Controls, All Kinds (Assayed)1 recall0 reports
- SP CONTROL 1 PS2682Randox Laboratories Limited · Multi-Analyte Controls, All Kinds (Assayed)1 recall0 reports
- BLOOD GAS CONTROL - LEVEL 2 (BG CONTROL 2) BG5002Randox Laboratories Limited · Multi-Analyte Controls, All Kinds (Assayed)1 recall0 reports
- LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM PLUS - LEVEL 3 (LIQ CHEM ASY PREMIUM PL LAE4215Randox Laboratories Limited · Multi-Analyte Controls, All Kinds (Assayed)1 recall0 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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