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Centurion 66695Recalls & reported problems

Centurion Medical Products Corporation · STERILE STRT KELLY HEMOSTAT (SK8039S) · Class 1

2 open recalls name 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
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 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. Nov 12, 2024Open, Classified

    Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.

    Z-0754-2025 · Root cause: Process control · FDA record ↗

  2. Feb 23, 2024Open, Classified

    Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

    Z-1438-2024 · Root cause: Process control · FDA record ↗

Other HEMOSTAT devices

All HEMOSTAT devices →

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