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QC Sets and Panels: KWIK-STIK™ 2 Pack 5112PRecalls & reported problems

Microbiologics Inc. · QC Sets and Panels: KWIK-STIK™ AST-GP (4 Strains) QC Set · Class 1

All models of QC Sets and Panels: KWIK-STIK 2 Pack (6)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records 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. Feb 18, 2020Class IITerminated

    Tests returning incorrect susceptible results. High Level Gentamicin Synergy value was out of specification (sensitive) when analyzed on the Vitek 2 AST-GP67 card, and these lots failed the disk diffusion method used for product release.

    Z-0588-2022 · Root cause: Process design · Recall details · FDA record ↗

  2. Feb 18, 2020Class IITerminated

    Tests returning incorrect susceptible results. High Level Gentamicin Synergy value was out of specification (sensitive) when analyzed on the Vitek 2 AST-GP67 card, and these lots failed the disk diffusion method used for product release.

    Z-0587-2022 · Root cause: Process design · Recall details · FDA record ↗

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Sources and updates

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