Steris recalls

Steris has 113 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 24 Jun 2026. 23 are still ongoing. 6 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls113since 2012
Last 12 months6reported
Class I00% of total
Ongoing23latest 24 Jun 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 109 96%Class III 4 4%

By year

Ongoing steris recalls

23 active

All steris recalls, newest first

113 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIAlyon Surgical Lighting System recalled by SterisSterisOtherNationwide
DeviceCLASS IIHarmonyAIR A-Series Surgical Lighting System recalled by SterisSterisOtherNationwide
DeviceCLASS IIHarmonyAIR A-Series Surgical Lighting System recalled by SterisSterisOtherNationwide
DeviceCLASS IIBarco MNA with the HexaVue IP Integration System recalled by SterisSterisOtherNationwide
DeviceCLASS IIThe Amsco 7053HP Washer/Disinfector is intended for use recalledSterisForeign MaterialNationwide
DeviceCLASS IIThe Amsco 7052HP Washer/Disinfector is intended for use recalledSterisForeign MaterialNationwide
DeviceCLASS IIDual Flat Panel Monitor (DFPM) accessories recalled by SterisSterisOtherNationwide
DeviceCLASS IIDual Flat Panel Monitor (DFPM) accessories recalled by SterisSterisOtherNationwide
DeviceCLASS IIHookups provide the interface between DSD Automated recalled by SterisSterisOtherNationwide
DeviceCLASS IIHookups provide the interface between an Advantage Plus" recalledSterisOtherNationwide
DeviceCLASS IIHookups provide the interface between an Advantage Plus" recalledSterisOtherNationwide
DeviceCLASS IIHookups provide the interface between an Advantage Plus" recalledSterisOtherNationwide
DeviceCLASS IIDual Articulating Headrest, Velcro recalled by SterisSterisDevice MalfunctionNationwide
DeviceCLASS IIDual Articulating Headrest, Pad Ret recalled by SterisSterisDevice MalfunctionNationwide
DeviceCLASS IIV. Mueller Universal Bandage Scissors Black Plastic Handles recalledSterisSterilityNationwide
DeviceCLASS IIHookup Accessories used with Medivators Advantage Plus recalledSterisOtherNationwide
DeviceCLASS IIReliance Vision Multi-Chamber Washer/Disinfector recalled by SterisSterisDevice MalfunctionNationwide
DeviceCLASS IILighting and Visualization Systems recalled by SterisSterisSterilityNationwide
DeviceCLASS IILighting and Visualization Systems recalled by SterisSterisSterilityNationwide
DeviceCLASS IIVerify Dual Species Self-Contained Biological Indicators recalledSterisSterilityNationwide
DeviceCLASS IIVerify Steam Test Pack (20 Tests and 5 controls) recalled by SterisSterisSterilityNationwide
DeviceCLASS IIVerify Dual Species Self-Contained Biological Indicators recalledSterisSterilityNationwide
DeviceCLASS IIVerify Steam Test Pack (20 Tests and 20 controls) recalled by SterisSterisSterilityNationwide
DeviceCLASS IIGI4000 Electrosurgical Unit recalled by SterisSterisDevice MalfunctionNationwide
DeviceCLASS IIHu-Friedy K360 Scalpel Handle, 360 Degree Scalpel Handle recalledSterisChoking Hazard5 states
DeviceCLASS IIReliance Synergy Washer/Disinfector recalled by SterisSterisDevice MalfunctionNationwide
DeviceCLASS IIUltra Pure Non-Woven Sponges Non-Sterile 4-Ply 2 10 sleeves recalledSterisHidden Drug IngredientsNationwide
DeviceCLASS IIUltra Pure Non-Woven Sponges Non-Sterile 4-Ply 5 25 sleeves recalledSterisHidden Drug IngredientsNationwide
DeviceCLASS IIOT1000 Series Orthopedic Surgical Tables recalled by SterisSterisOther39 states
DeviceCLASS IIReliance Vision Single-Chamber Washer/Disinfector recalled by SterisSterisDevice MalfunctionNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.