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Transystem™ 900-0370Recalls & reported problems

Copan Italia SPA · TRANSYSTEM LQ STUART DUAL APPLICATOS BREAKABLE POINT 33mm · Class 1

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

Recalls naming this device

  1. Jun 20, 2024Open, Classified

    Specimen collection device may leak after the patient sample swabs have been inserted into the test tubes, which could result in biohazard exposure, cross contamination causing false positive results for other specimens, and/or delay to test results.

    Z-2584-2024 · Root cause: Under Investigation by firm · FDA record ↗

Other Culture Media, Non-Propagating Transport devices

All Culture Media, Non-Propagating Transport devices →

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