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Medical Device

VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007

Recall date: 2026-10-14 · Source: FDA_DEVICE
Brand / Firm
Steris Corporation
Product
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007
Reason for recall
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator will show no growth, indicating that the steam cycle was effective, even if the steam cycle did not achieve the intended spore reduction
Units affected
409
Description
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007
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