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KWIK-STIK™ 01145URecalls & reported problems

Microbiologics Inc. · KWIK-STIK™ K. pneumoniae NCTC 13443 · Class 1

All models of KWIK-STIK (20)

Data updated Oct 16, 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 16, 2026.

Recalls naming this device

  1. Oct 8, 2020Terminated

    KWIK-STIK 6 Pack Klebsiella pneumoniae derived from NCTC 13443 (Catalog# 01145K) should contain the NDM-1 positive strain, but was confirmed to be NDM-1 negative.

    Z-0303-2021 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

  2. Oct 8, 2020Terminated

    KWIK-STIK 2 Pack Klebsiella pneumoniae derived from NCTC 13443 (Catalog# 01145P) should contain the NDM-1 positive strain, but was confirmed to be NDM-1 negative.

    Z-0302-2021 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

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Sources and updates

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