Brand

Steris Corporation: official recall notices

10 official recall or safety notices on this site name Steris Corporation, dated between 2024-06-13 and 2026-09-23. They were issued by 1 authority: US FDA — Medical Devices (10).

Countries where the notices were issued: United States (10).

Name as written in the notices: Steris Corporation. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.

Notices by year

Year	Notices
2026	7
2024	3

Notices by authority

Authority	Notices
US FDA — Medical Devices	10

All notices

Date	Authority	Product	Hazard (as classified)
2026-09-23	US FDA — Medical Devices	HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgical video	—
2026-08-31	US FDA — Medical Devices	VERIFY Biological Steam Test Pack Model/Catalog Number: S3065	—
2026-08-31	US FDA — Medical Devices	VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006	—
2026-08-31	US FDA — Medical Devices	VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061	—
2026-08-31	US FDA — Medical Devices	VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060	—
2026-08-31	US FDA — Medical Devices	VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007	—
2026-08-31	US FDA — Medical Devices	VERIFY Biological Steam Test Pack Model/Catalog Number: S3069	—
2024-06-13	US FDA — Medical Devices	Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide the interface between an Advantage Plus	—
2024-06-13	US FDA — Medical Devices	Hookup Model/Catalog Number: 2-8-540 Product Description: Hookups provide the interface between an Advantage Plus" A	—
2024-06-13	US FDA — Medical Devices	Hookup Model/Catalog Number: 2-8-540HAN Product Description: Hookups provide the interface between an Advantage Plus	—

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