Steris recalls
14 federal recalls on file, showing the 7 from the last 12 months. We read every CPSC, FDA, USDA and NHTSA notice for Steris and put it in plain English.
Recent recalls
Steris RAPICIDE PA disinfectant recalled for pressurized bottle riskThe vented cap on this high-level disinfectant bottle can become blocked, causing gas to build up inside. When the pressure increases, the bottle may swell, and opening it could release vapor or liquid that may expose users to the chemical if protective equipment is not properly worn.
ModerateFDAOct 21, 20263 products
- Steris HexaVue Focus system recalled for patient data mismatch on prints
A software issue in Steris HexaVue Focus Integration System (version 2.0.18) can cause incorrect patient information to appear on manually printed surgical images. This mismatch could lead to documentation errors or clinical images being linked to the wrong patient record.
ModerateFDAOct 14, 2026
- Steris VERIFY biological indicators recalled for spore shelf-life issue
Steris is recalling six VERIFY biological indicator and challenge pack products used to monitor steam sterilization cycles. The spore population in these products may fall below its minimum shelf-life specification, so an indicator could show no growth even when a steam cycle did not achieve the intended spore reduction. No injuries have been reported.
ModerateFDAOct 14, 20266 products
- Steris HarmonyAIR, ALYON surgical lights recalled over detaching buttons
Steris is recalling two surgical lighting systems, HarmonyAIR A-Series and ALYON, totaling about 2,650 units. The plus and minus buttons used to adjust light intensity on the light heads may detach. No injuries have been reported.
ModerateFDAJun 24, 20262 products
- Steris HarmonyAIR surgical lights recalled for paint chipping
Paint on the light heads of Steris HarmonyAIR A-Series Surgical Lighting Systems may chip or peel. This could potentially affect the lighting system's performance or introduce debris into the surgical field. The FDA has classified this as a Class II recall.
ModerateFDAJun 24, 2026
- Check your Steris Barco MNA adapter serial number
Steris Corporation identified that a limited batch of MNA-6x0 adapter components used in the Barco MNA with HexaVue IP Integration System were manufactured with an incorrect configuration file. This affects 10 units with specific serial numbers distributed across seven states.
ModerateFDAFeb 18, 2026
- Contact Steris about AMSCO 7052HP washer
A wire in the electrical box of the AMSCO 7052HP Washer/Disinfector may shift out of position, causing electrical arcing inside the unit. The arcing occurs internally and does not pose a shock risk to users, but could affect equipment function or safety.
ModerateFDADec 17, 20252 products