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KWIK-STIK™ 01023URecalls & reported problems

Microbiologics Inc. · KWIK-STIK™ C. coli ATCC 33559™ · Class 1

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. Mar 25, 2013Terminated

    Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7, contained an inner label stating the product is Catalog #0919K Haemophilus influenza. The organism has been confirmed to be C. coli, indicating this is a labeling error and the organism is the correct organism.

    Z-0641-2022 · Root cause: Labeling mix-ups · FDA record ↗

Other KIT, QUALITY CONTROL FOR CULTURE MEDIA devices

All KIT, QUALITY CONTROL FOR CULTURE MEDIA devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.