Steris Corporation Recalls

10 recalls on record in the United States

medical: 10
medical Class II
2026-06-24

Steris Corporation recalls HarmonyAIR A-Series Surgical Lighting System

The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

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medical Class II
2026-06-24

Steris Corporation recalls HarmonyAIR A-Series Surgical Lighting System

There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.

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medical Class II
2026-06-24

Steris Corporation recalls ALYON Surgical Lighting System

The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

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medical Class II
2026-10-14

Steris Corporation recalls VERIFY Biological Steam Test Pack Model/Catalog Number: S30

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

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medical Class II
2026-10-14

Steris Corporation recalls VERIFY Biological/Integrator Challenge Pack Model/Catalog

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

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medical Class II
2026-10-14

Steris Corporation recalls VERIFY Dual Species Self-Contained Biological Indicator Mod

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

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medical Class II
2026-10-14

Steris Corporation recalls VERIFY Dual Species Self-Contained Biological Indicator M

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

View recall details →

medical Class II
2026-10-14

Steris Corporation recalls VERIFY Biological/Integrator Challenge Pack Model/Catalog

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

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medical Class II
2026-10-14

Steris Corporation recalls HexaVue Focus Integration System, a single, all-in-one syste

A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on printed images could create a documentation discrepancy or incorrect association of clinical images with a patient record.

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medical Class II
2026-10-14

Steris Corporation recalls VERIFY Biological Steam Test Pack Model/Catalog Number: S30

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

View recall details →