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KWIK-STIK™ 0323URecalls & reported problems

Microbiologics Inc. · KWIK-STIK™ E. cloacae ATCC 13047™ · Class 1

Data updated Oct 13, 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Feb 24, 2021Terminated

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

    Z-0544-2022 · Root cause: Labeling mix-ups · FDA record ↗

Other KIT, QUALITY CONTROL FOR CULTURE MEDIA devices

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Sources and updates

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