Liquichek 171Recalls & reported problems
Bio-Rad Laboratories, Inc. · Liquichek Diabetes Control Level 1 (A human whole blood assayed diabetes control.) · Class 2
Data updated Oct 13, 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 00847661000839), received between Sep 25, 2018 and Sep 25, 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 25, 2018Human-Device Interface Problem; Human-Device Interface Problem
ON SEPTEMBER 06, 2018, BIO-RAD QSD, (B)(4) RECEIVED A REPORT FOR A POTENTIAL ADVERSE EVENT WHERE A LABORATORY TECHNICIAN SPLASHED LIQUICHEK DIABETES CONTROL LOT # 38560 INTO HER EYE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7906291 ↗
Other CONTROL, HEMOGLOBIN devices
- Eurotrol 171.003.002Eurotrol B.V. · Control, Hemoglobin1 recall0 reports
- Eurotrol 171.001.002Eurotrol B.V. · Control, Hemoglobin1 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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