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iVIEW DAB Detection Kit 05266173001Recalls & reported problems

Ventana Medical Systems, Inc. · Class 1

All models of iVIEW DAB Detection Kit (2)

Data updated Oct 18, 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 18, 2026.

Recalls naming this device

  1. Aug 2, 2018Class ITerminated

    Leaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers. A false negative IHC result may occur.

    Z-3001-2018 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

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Sources and updates

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