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KWIK-STIK™ 0805URecalls & reported problems

Microbiologics Inc. · KWIK-STIK™ B. diminuta ATCC 19146™ · Class 1

All models of KWIK-STIK (20)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

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, 1 still open.

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. Jun 17, 2025Open, Classified

    Affected products contain Staphylococcus epidermidis instead of the expected Brevundimonas diminuta. This may cause the user's quality control to fail and delayed diagnosis for the patient.

    Z-2124-2025 · Root cause: Under Investigation by firm · 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