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KWIK-STIK™ 0726URecalls & reported problems

Microbiologics Inc. · KWIK-STIK™ C. parapsilosis ATCC 22019™ · 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
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

  1. Feb 24, 2021Terminated

    Potential that products packaged for lot 726-57-10 were packaged in pouches labeled as 323-108-7.

    Z-0543-2022 · Root cause: Labeling mix-ups · Recall details · FDA record ↗

Other KIT, QUALITY CONTROL FOR CULTURE MEDIA devices

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page