PlainRecalls

Steris Corporation

Compiled from official public sources by the publisher.

112 recalls on record · Latest: Jun 24, 2026

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Agency notice ledger

Federal filing book Steris Corporation HEAVY-BOOK · SINGLE-AGENCY

#148 of 14,151 · 112 notices · 0.107% archive

  • BOOK 112 notices
  • RANK #148 of 14,151
  • SHARE 0.107% archive
  • AGENCY FDA Devices (112)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 24, 2026
  • PHOTO Carefusion 2200 Inc

Nearest notice-volume peer: Carefusion 2200 Inc (0 notice gap)

Steris Corporation accounts for about 0.107% of the 104,423-notice archive on 112 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Steris Corporation sits among 14,151 recalling firms

Steris Corporation ranks 148th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Steris Corporation vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

112 148th of 14151 higher than 14,003 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Steris Corporation in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Steris Corporation holds about 0.107% of archive notices alongside 112 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Nov 13, 2013

Harmony Equipment Management System, Model #603X/80XX, STERIS Corporation, Mentor, OH Harmony Equipment Management Systems (EMS) are used in hospital facilities to provide ready access to medical gasses, electrical power and audio/visual data services, in addition to managing surgical support equipment such as endoscopic equipment, cautery devices and insufflators.
FDA Devices Moderate Oct 2, 2013

Reliance Endoscope Processing System (REPS), STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060-1834 USA www.steris.com. The intended use of the REPS is washing and high level disinfection of up to two manually pre-cleaned, immersible, reusable, heat-resistant, semi-critical devices.
FDA Devices Moderate Jul 31, 2013

STERIS Fine Traction Device, one unit per box Product Usage: The Fine Traction Device is used to provide traction and enable fine adjustments to traction and orientation of the leg during orthopedic procedures.
FDA Devices Moderate Jul 3, 2013

Quick Connect QLC1677E, QRC1699E, QPC1721E and QFC1683E. STERIS Corporation, Mentor, OH 44060 QLC1677E, QRC1699E, QPC1721E and QFC1683E contain processing instructions, a Quick Reference Wall Chart and a flow unit. The flow unit consists of a Quick Reference Card, tubing, tethers and adapters for connecting specified devices to Flexible Processing Trays/Containers.
FDA Devices Moderate Mar 13, 2013

AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization of heat and moisture-stable materials used in healthcare facilities.
FDA Devices Moderate Sep 26, 2012

STERIS 5085 and 5085 SRT Surgical Tables, Product Usage: The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal table top elevation. It accommodates all general surgical procedures including but not limited to, cardiac and vascular, endoscopic, gynecology, urology, nephrectomy, neurology, ophthalmologic, orthopedics and other procedures requiring intraoperative fluoroscopic C-arm imaging and also supports laparoscopic surgical

FDA Devices Moderate Sep 26, 2012

Verify¿ Bowie-Dick Test Card, Model #S3098, Steris Biological Operations, 9325 Pinecone Drive, Mentor, OH 44060 The Verify Bowie-Dick Test Card consists of a card printed on one side with bars of chemical indicator ink. On the opposite side of the card, space is provided for critical cycle information to be recorded. The card is laminated inside a thin clear plastic enclosure. The enclosure has two holes in it to allow air removal and steam penetration. The preassembled test is used to evalua
FDA Devices Moderate Sep 26, 2012

A mobile, electro-hydraulically operated, fluoroscopic/C-Arm compatible general surgical table. Product Usage: Product provides a flexible, easy-to-use, articulated posturing of a patient for either general, I.A., or specialized surgical procedures. There are movable components and accessories intended for use during diagnostic examinations or surgical procedures to support and position a patient.
FDA Devices Moderate Sep 19, 2012

The SYSTEM 1E Liquid Sterilant Processing System. The SYSTEM 1E Liquid Sterilant Processing System is intended for the liquid chemical sterilization of manually cleaned immersible and reusable critical and semi-critical heat sensitive medical devices, including endoscopes and their accessories.
FDA Devices Low Sep 12, 2012

100 ft roll of tubing inside a cardboard box. Medical devices are sealed into the tubes prior to ethylene oxide sterilization. Tube maintains sterility of the enclosed medical devices until opened.
FDA Devices Moderate Sep 5, 2012

QKC1692E The QKC1692E Quick Connect device connects endoscopes to the sterilization tray for C1220E liquid chemical sterilization processor.
FDA Devices Moderate Aug 8, 2012

The Reliance 130 and 130L Cart Washer/Disinfector is a high capacity mechanical washer intended for use in the washing, low-level disinfecting, and drying of carts, utensils, beds and other miscellaneous reusable items used in the care of patients at healthcare facilities / Crated for shipping.

Steris Corporation carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (112 here — heavy-book).

Carefusion 2200 Inc 112 Aomori Olympus Co., Ltd. 113 Herbal Doctor Remedies 113 Rabbit Creek Products Inc. 114 Mitsubishi 115

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Carefusion 2200 Inc 112 Aomori Olympus Co., Ltd. 113 Raysearch Laboratories Ab 115 Stryker Corporation 115

Frequently Asked Questions

How many federal recall notices name Steris Corporation? ▼
PlainRecalls indexes 112 distinct federal recall events naming Steris Corporation, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Steris Corporation sit among other recalling firms? ▼
Steris Corporation ranks #148 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Steris Corporation's notices? ▼
FDA Devices accounts for 112 of this firm's 112 indexed notices.
What product category dominates Steris Corporation's filing book? ▼
Filings for Steris Corporation span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Steris Corporation: 112 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Steris Corporation; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026