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VERIFY S3065 (UDI 10724995023840)Recalls & reported problems

Steris Corporation · The VERIFY Disposable Biological Steam Test Pack is a single use test pack designed for monitoring the effectiveness of common steam sterilizing processes, including 250 degrees F (121 degrees C) gravity cycles and 270 degrees F (132 C) prevacuum cycles. 20 Packs with 5 Controls. · Class 2

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. Dec 12, 2022Open, Classified

    Biological indicator (BI) used to promote growth of the G. stearothermophilus and B. atrophaeus spores was inconsistent in promoting growth throughout lot , some BIs within the lot performed as intended while others did not. When used to monitor steam and ethylene oxide sterilization cycles, the potential hazard is that the BI will show no growth indicating that the cycle was effective, even if it may not have been.

    Z-0780-2023 · Root cause: Employee error · FDA record ↗

Other Indicator, biological sterilization process devices

All Indicator, biological sterilization process devices →

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