Steris Corporation recalls
15 recalls.
- RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - HexaVue Focus Integration System recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on printed images... - VERIFY Biological Steam Test Pack Model/Catalog Number: S3069 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological Steam Test Pack Model/Catalog Number: S3065 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - ALYON Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. - HarmonyAIR A-Series Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. - HarmonyAIR A-Series Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads. - AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product... recall (Steris Corporation)
Medical deviceClass IIReported December 17, 2025 · Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within... - AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description:... recall (Steris Corporation)
Medical deviceClass IIReported December 17, 2025 · Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within...