Fresh Recalls

Steris recalls

10 recent recalls on record for Steris in connected official government data as of October 22, 2026 at 12:00 PM UTC.

Models with recalls

ALYON Surgical Lighting System (1)HarmonyAIR A-Series Surgical Lighting System (2)HexaVue Focus Integration System (1)VERIFY Biological Steam Test Pack Model/Catalog Number (2)VERIFY Biological/Integrator Challenge Pack Model/Catalog Number (2)VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number (2)

All Steris recalls

FDA Class II · Medical device · October 14, 2026

HexaVue Focus Integration System recall — Steris Corporation

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 docum…

Official ID Z-0118-2027 · Official record ↗

FDA Class II · Medical device · October 14, 2026

VERIFY Biological Steam Test Pack Model/Catalog Number recall — Steris Corporation

Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…

Official ID Z-0075-2027 · Official record ↗

FDA Class II · Medical device · October 14, 2026

VERIFY Biological Steam Test Pack Model/Catalog Number recall — Steris Corporation

Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…

Official ID Z-0074-2027 · Official record ↗

FDA Class II · Medical device · October 14, 2026

VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number recall — Steris Corporation

Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…

Official ID Z-0073-2027 · Official record ↗

FDA Class II · Medical device · October 14, 2026

VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number recall — Steris Corporation

Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…

Official ID Z-0072-2027 · Official record ↗

FDA Class II · Medical device · October 14, 2026

VERIFY Biological/Integrator Challenge Pack Model/Catalog Number recall — Steris Corporation

Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…

Official ID Z-0071-2027 · Official record ↗

FDA Class II · Medical device · October 14, 2026

VERIFY Biological/Integrator Challenge Pack Model/Catalog Number recall — Steris Corporation

Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…

Official ID Z-0070-2027 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ALYON Surgical Lighting System recall — Steris Corporation

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

Official ID Z-2450-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

HarmonyAIR A-Series Surgical Lighting System recall — Steris Corporation

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

Official ID Z-2449-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

HarmonyAIR A-Series Surgical Lighting System recall — Steris Corporation

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

Official ID Z-2448-2026 · Official record ↗

Verify with the official sources:

Found something wrong or missing? Report a data error.

Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.