PlainRecalls

Steris Corporation

Compiled from official public sources by the editorial team.

109 recalls on record · Latest: Feb 18, 2026

Steris Corporation Recall Insight

Steris Corporation appears on 109 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.107% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Feb 18, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 49 moderate, and 1 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Sep 12, 2018 to Feb 18, 2026.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Feb 18, 2026

Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H

FDA Devices Moderate Dec 17, 2025

AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector is intended for use in the…

FDA Devices Moderate Dec 17, 2025

AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description: The AMSCO 7053HP Washer/Disinfector is intended for use in th…

FDA Devices Moderate Aug 6, 2025

Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical Lighting Systems

FDA Devices Moderate Aug 6, 2025

Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR A-Series Surgical Lighting Systems

FDA Devices Moderate Aug 14, 2024

Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide the interface between an Advantage Plus" Automated Endoscope Reproce…

FDA Devices Moderate Aug 14, 2024

Hookup Model/Catalog Number: 2-8-540 Product Description: Hookups provide the interface between an Advantage Plus" Automated Endoscope Reprocesso…

FDA Devices Moderate Aug 14, 2024

Hookup Model/Catalog Number: 2-8-540HAN Product Description: Hookups provide the interface between an Advantage Plus" Automated Endoscope Reproce…

FDA Devices Moderate Aug 14, 2024

Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide the interface between DSD Automated Endoscope Reprocessors ( AER…

FDA Devices Moderate Feb 14, 2024

Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754

FDA Devices Moderate Feb 14, 2024

Dual Articulating Headrest, Velcro P/N P141210813, REF BF753

FDA Devices Moderate Jan 24, 2024

V. Mueller Universal Bandage Scissors Black Plastic Handles Heavy-Duty, Autoclavable, Overall Length 7 (18 cm)- Intended to cut through tape and ban…

FDA Devices Moderate Jan 3, 2024

Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS Pass Thru Automated Endoscope Reprocessors Model # Model Description 2…

FDA Devices Moderate May 24, 2023

Reliance Vision Multi-Chamber Washer/Disinfector, Reference Number FH83062

FDA Devices Moderate May 10, 2023

Steris Lighting and Visualization Systems, Sterile Light Handle Cover (LB53)- Surgical light handle covers, including disposable surgical light handl…

FDA Devices Moderate May 10, 2023

Steris Lighting and Visualization Systems, Sterile Light handle Cover LB44 -Sterilizable consumables (disposable, single use) used to drape the lig…

FDA Devices Moderate Jan 11, 2023

VERIFY Steam Test Pack (20 Tests and 20 controls) Item Number: S3069 Intended for use in installation testing and routine monitoring of steam and…

FDA Devices Moderate Jan 11, 2023

VERIFY Dual Species Self-Contained Biological Indicators, 100 per box Item Number: S3061 Intended for use in installation testing and routine mon…

FDA Devices Moderate Jan 11, 2023

VERIFY Steam Test Pack (20 Tests and 5 controls) Item Number: S3065 Intended for use in installation testing and routine monitoring of steam and …

FDA Devices Moderate Jan 11, 2023

VERIFY Dual Species Self-Contained Biological Indicators, 50 per box Item Number: S3060 Intended for use in installation testing and routine moni…

FDA Devices Moderate Nov 23, 2022

GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to perform cutting and/or coagulation and coagulation with or without deliv…

FDA Devices Moderate Oct 19, 2022

Hu-Friedy K360 Scalpel Handle, 360 Degree Scalpel Handle, REF K360

FDA Devices Moderate Jun 15, 2022

Reliance Synergy Washer/Disinfector

FDA Devices Moderate Jun 1, 2022

Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5,000 per case 25 sleeves of 200 2 in x 2 in / 5.1 cm x 5.1 cm Model Number: ENC100

FDA Devices Moderate Jun 1, 2022

Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 2,000 per case 10 sleeves of 200 4 in x 4 in / 10.2 cm x 10.2 cm Model Number: ENC4100

FDA Devices Moderate Mar 3, 2021

OT1000 Series Orthopedic Surgical Tables

FDA Devices Moderate Jan 27, 2021

Reliance Vision Single-Chamber Washer/Disinfector - Product Usage: intended for use in the cleaning and intermediate level disinfection of soiled reu…

FDA Devices Moderate Jan 20, 2021

Medisafe Distal Duck Kit and Duck Bag, Cleaner, ultrasonic, medical instrument - Product Usage: intended to keep instruments moist during transportat…

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temp 7.5"x13.5" Heat Seal Pouch 200 pouches per box; 5 boxes per case Model Number: 883713

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temperature Tubing 9"x100'. One roll per box; 10 boxes per case 6 rolls/cs Model Number: 881091

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temp 13"x18" Self Seal Pouch 100 pouches per box; 4 boxes per case Model Number: 884118

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temp 3.5"x9" Self Seal Pouch 200 pouches per box; 4 boxes per case Model Number: 884039

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temp 6"x10" Heat Seal Pouch 200 pouches per box; 5 boxes per case Model Number: 883610

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temperature Tubing 6"x100'. One roll per box; 10 boxes per case 10 rolls/cs Model Number: 881061

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temp 5.5"x10" Self Seal Pouch 200 pouches per box; 4 boxes per case Model Number: 884510

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box; 4 boxes per case Model Number: 884411

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temp 5"x15" Self Seal Pouch 200 pouches per box; 4 boxes per case Model Number: 884515

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box; 4 boxes per case Model Number: 884816

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box; 4 boxes per case Model Number: 884713

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temp 4.5"x11" Heat Seal Pouch 200 pouches per box; 5 boxes per case Model Number: 883411

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temperature Tubing 3"x100'. One roll per box; 10 boxes per case 10 rolls/cs Model Number: 881031

FDA Devices Moderate Jan 13, 2021

Vis-U-All High Temperature Tubing 4"x100'. One roll per box; 10 boxes per case 10 rolls/cs Model Number: 881041

FDA Devices Low Nov 25, 2020

Olympus Leak Test Adapter used with Acu-sInQ Complete Endoscope Cleaning Aid Systems-intended to assist manual flexible endoscope cleaning Part num…

FDA Devices Moderate Aug 5, 2020

InnoWave Sonic Irrigator, There are currently six models (PCF, Pro, Ultra, Ultra+, Unity, and ECO) - Product Usage: STERIS InnoWave Sonic Irrigators …

FDA Devices Moderate Dec 11, 2019

Evolution Loading Car and Transfer Carriage- Accessory to the Sterilizer, Steam

FDA Devices Moderate Dec 11, 2019

Eagle 3000 Sterilizer, small steam sterilizer. Product Usage: The Eagle 3000 Small Sterilizer is designed for sterilization of certain materials used…

FDA Devices Moderate Mar 20, 2019

AMSCO 5000 Series Washer/Disinfector Model # 5052

FDA Devices Moderate Mar 20, 2019

AMSCO 3000 Series Washer/Disinfector Model # 3052

FDA Devices Moderate Feb 20, 2019

ATLAS Loading Car

FDA Devices Moderate Sep 12, 2018

AMSCO V-PRO 1, V-PRO 1 Plus, and V-PRO maX Low Temperature Sterilization Systems The V-PRO 1, V-PRO 1 Plus, and V-PRO maX Low Temperature Sterili…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Steris Corporation with Zimmer Biomet, Inc. →

Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.