SP CAL (LIQ) IT2692Recalls & reported problems
Randox Laboratories Limited · Liquid Protein Calibrators are an in vitro diagnostic product used for the calibration of Alpha-1-Antitrypsin, Alpha-1-Acid glycoprotein, IgA, IgG and IgM assays that require sample pre-dilution. · Class 2
All models of SP CAL (LIQ) (2)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
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.
Recalls naming this device
- Nov 19, 2018Terminated
Calibrator value sheets have been modified for assigned value of Alpha-1-Acid-Glycoprotein (AGP), IgA and IgG to improve the alignment. IgG measurement reference has also been corrected.
Z-0660-2019 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other Calibrator, Multi-Analyte Mixture devices
- CAL 3 CAL2351Randox Laboratories Limited · Calibrator, Multi-Analyte Mixture6 recalls0 reports
- VITROS 6844508Ortho-Clinical Diagnostics, Inc. · Calibrator, multi-analyte mixture2 recalls7 reports
- SP CAL (LIQ) IT2691Randox Laboratories Limited · Calibrator, Multi-Analyte Mixture2 recalls0 reports
- VITROS 1662659Ortho-Clinical Diagnostics, Inc. · CALIBRATOR, MULTI-ANALYTE MIXTURE1 recall17 reports
- RAPIDPoint® 500 Measurement Cartridge 10491449Siemens Healthcare Diagnostics Inc. · CALIBRATOR, MULTI-ANALYTE MIXTURE1 recall3 reports
- ADVIA® Chemistry Calibrator 10312279Siemens Healthcare Diagnostics Inc. · CALIBRATOR, MULTI-ANALYTE MIXTURE1 recall3 reports
- Dimension Vista® LOCI 8 CAL 10488192Siemens Healthcare Diagnostics Inc. · CALIBRATOR, MULTI-ANALYTE MIXTURE1 recall0 reports
- RAPIDPoint® 500 Measurement Cartridge 10491447Siemens Healthcare Diagnostics Inc. · CALIBRATOR, MULTI-ANALYTE MIXTURE1 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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