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Medium risk Drugs & MedicationsClass II

Steris Corporation Recall

VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060

Updated August 31, 2026

Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060. Hazard: 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

Is the Steris Corporation recalled? Yes. This product was recalled by FDA on August 31, 2026. Details below.

What is recalled

VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

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

Brands affected

Steris Corporation
Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-0072-2027
Classification
Class II
Recalled
August 31, 2026
Read the official notice

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