AutoDELFIA Plate processor 1235-0110Recalls & reported problems
Wallac Oy · Used with 1235-5110 AutoDELFIA® Plate Processor System or 1235-5220 AutoDELFIA® System (SP and PP). · Class 1
- 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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Dec 21, 2016Terminated
AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Z-1100-2017 · Root cause: Software design · FDA record ↗
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- VITROS 1922814Ortho-Clinical Diagnostics, Inc. · FLUOROMETER, FOR CLINICAL USE1 recall10 reports
- VITROS 6801059Ortho-Clinical Diagnostics, Inc. · FLUOROMETER, FOR CLINICAL USE1 recall1 report
- AUTOMATED ENZYME IMMUNOASSAY ANALYZER AIA-2000 LATosoh Corporation · Fluorometer, For Clinical Use35 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.