--- title: "Steris Corporation Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Steris Corporation recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/steris-corporation/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Steris Corporation recall records **23** reported ongoing 28 records in this archive. Latest source date May 15, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status May 15, 2026 FDA device enforcement ### [HarmonyAIR A-Series Surgical Lighting System](https://isitonrecall.com/recall/fda-device-z-2448-2026-harmonyair-a-series-surgical-lighting-system/) There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Canada, India, New Zealand, Panama. [Official source for HarmonyAIR A-Series Surgical Lighting System](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2448-2026%22) May 15, 2026 FDA device enforcement ### [HarmonyAIR A-Series Surgical Lighting System](https://isitonrecall.com/recall/fda-device-z-2449-2026-harmonyair-a-series-surgical-lighting-system/) The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for HarmonyAIR A-Series Surgical Lighting System](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2449-2026%22) May 15, 2026 FDA device enforcement ### [ALYON Surgical Lighting System](https://isitonrecall.com/recall/fda-device-z-2450-2026-alyon-surgical-lighting-system/) The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for ALYON Surgical Lighting System](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2450-2026%22) Nov 19, 2025 FDA device enforcement ### [AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector is intended for use in the cleaning and intermediate-level ...](https://isitonrecall.com/recall/fda-device-z-0909-2026-amsco-7052hp-washer-disinfector-model-catalog-number-7052hp-product-description-the-amsco-7052hp-was/) Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users). Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of Arizona, Colorado, Florida, Georgia, Illinois, Kentucky, Louisiana, Michigan, New Hampshire, New York, North Carolina, Pe... [Official source for AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052H...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0909-2026%22) Nov 19, 2025 FDA device enforcement ### [AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description: The AMSCO 7053HP Washer/Disinfector is intended for use in the cleaning and intermediate-level ...](https://isitonrecall.com/recall/fda-device-z-0910-2026-amsco-7053hp-washer-disinfector-model-catalog-number-7053hp-product-description-the-amsco-7053hp-was/) Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users). Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of Arizona, Colorado, Florida, Georgia, Illinois, Kentucky, Louisiana, Michigan, New Hampshire, New York, North Carolina, Pe... [Official source for AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description: The AMSCO 7053H...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0910-2026%22) Jun 23, 2025 FDA device enforcement ### [Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR A-Series Surgical Lighting Systems](https://isitonrecall.com/recall/fda-device-z-2177-2025-dual-flat-panel-monitor-dfpm-accessories-for-harmonyair-a-series-surgical-lighting-systems/) The DFPM yoke assembly ("yoke assembly") may detach from the spring arm. Should the yoke assembly detach from the spring arm, the yoke assembly would not be expected to fully detach but rather hang from the wiring within the yoke assembly. Class II Reported ongoing Distribution: Worldwide - US Nationwide and Puerto Rico and the country of Canada. [Official source for Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR A-Series Surgical Lighting Systems](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2177-2025%22) Jun 23, 2025 FDA device enforcement ### [Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical Lighting Systems](https://isitonrecall.com/recall/fda-device-z-2178-2025-dual-flat-panel-monitor-dfpm-accessories-for-harmonyair-e-series-surgical-lighting-systems/) The DFPM yoke assembly ("yoke assembly") may detach from the spring arm. Should the yoke assembly detach from the spring arm, the yoke assembly would not be expected to fully detach but rather hang from the wiring within the yoke assembly. Class II Reported ongoing Distribution: Worldwide - US Nationwide and Puerto Rico and the country of Canada. [Official source for Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical Lighting Systems](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2178-2025%22) May 23, 2025 FDA device enforcement ### [Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H](https://isitonrecall.com/recall/fda-device-z-1361-2026-barco-mna-with-the-hexavue-ip-integration-system-model-catalog-number-mna-6x0-h/) This is a sub-recall of event RES 96885. The supplier identified that during their manufacturing process for a limited batch of MNA-6x0 (adapter) components the incorrect configuration file was used. Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, NC, NY, OH, TN, TX, and VA. [Official source for Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1361-2026%22) Jun 13, 2024 FDA device enforcement ### [Hookup Model/Catalog Number: 2-8-540 Product Description: Hookups provide the interface between an Advantage Plus" Automated Endoscope Reprocessor and Advantage Plus" Pass-Thru ...](https://isitonrecall.com/recall/fda-device-z-2536-2024-hookup-model-catalog-number-2-8-540-product-description-hookups-provide-the-interface-between-an-adv/) IFU for hookup were incorrectly reflected within hookup IFUs and online reference system, Hookup Lookup (HULU). Use of an incorrect hookup connection and/or parameter set may prevent an endoscope from being properly disinfected, which may present a risk of ... Class II Reported ongoing Distribution: Worldwide distribution - United States Nationwide and the countries of Canada, Belgium, Czech Republic, Denmark, Germany, Spain, Italy, Slovenia, Slovakia, Australia, Israel, Jo... [Official source for Hookup Model/Catalog Number: 2-8-540 Product Description: Hookups provide the interface between a...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2536-2024%22) Jun 13, 2024 FDA device enforcement ### [Hookup Model/Catalog Number: 2-8-540HAN Product Description: Hookups provide the interface between an Advantage Plus" Automated Endoscope Reprocessor and Advantage Plus" Pass-Th...](https://isitonrecall.com/recall/fda-device-z-2537-2024-hookup-model-catalog-number-2-8-540han-product-description-hookups-provide-the-interface-between-an/) IFU for hookup were incorrectly reflected within hookup IFUs and online reference system, Hookup Lookup (HULU). Use of an incorrect hookup connection and/or parameter set may prevent an endoscope from being properly disinfected, which may present a risk of ... Class II Reported ongoing Distribution: Worldwide distribution - United States Nationwide and the countries of Canada, Belgium, Czech Republic, Denmark, Germany, Spain, Italy, Slovenia, Slovakia, Australia, Israel, Jo... [Official source for Hookup Model/Catalog Number: 2-8-540HAN Product Description: Hookups provide the interface betwee...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2537-2024%22) Jun 13, 2024 FDA device enforcement ### [Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide the interface between an Advantage Plus" Automated Endoscope Reprocessor and Advantage Plus" Pass-Th...](https://isitonrecall.com/recall/fda-device-z-2538-2024-hookup-model-catalog-number-2-8-540cas-product-description-hookups-provide-the-interface-between-an/) IFU for hookup were incorrectly reflected within hookup IFUs and online reference system, Hookup Lookup (HULU). Use of an incorrect hookup connection and/or parameter set may prevent an endoscope from being properly disinfected, which may present a risk of ... Class II Reported ongoing Distribution: Worldwide distribution - United States Nationwide and the countries of Canada, Belgium, Czech Republic, Denmark, Germany, Spain, Italy, Slovenia, Slovakia, Australia, Israel, Jo... [Official source for Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide the interface betwee...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2538-2024%22) Jun 13, 2024 FDA device enforcement ### [Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide the interface between DSD Automated Endoscope Reprocessors ( AER ) and endoscopes, which allow p...](https://isitonrecall.com/recall/fda-device-z-2539-2024-hookup-model-catalog-number-dsd-110-hu0163-product-description-hookups-provide-the-interface-between/) IFU for hookup were incorrectly reflected within hookup IFUs and online reference system, Hookup Lookup (HULU). Use of an incorrect hookup connection and/or parameter set may prevent an endoscope from being properly disinfected, which may present a risk of ... Class II Reported ongoing Distribution: Worldwide distribution - United States Nationwide and the countries of Canada, Belgium, Czech Republic, Denmark, Germany, Spain, Italy, Slovenia, Slovakia, Australia, Israel, Jo... [Official source for Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide the interface be...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2539-2024%22) Dec 12, 2023 FDA device enforcement ### [Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754](https://isitonrecall.com/recall/fda-device-z-0983-2024-dual-articulating-headrest-pad-ret-p-n-p141210805-ref-bf754/) Dual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure which could result in an injury to the patient or a procedural delay. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AZ, CA, FL, IL, IN, IA, KS, LA, MN, MS, NV, NJ, OH, OK, OR, PA, TN, TX, UT, WA, WI & Puerto Rico, and the countries of Au... [Official source for Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0983-2024%22) Dec 12, 2023 FDA device enforcement ### [Dual Articulating Headrest, Velcro P/N P141210813, REF BF753](https://isitonrecall.com/recall/fda-device-z-0984-2024-dual-articulating-headrest-velcro-p-n-p141210813-ref-bf753/) Dual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure which could result in an injury to the patient or a procedural delay. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AZ, CA, FL, IL, IN, IA, KS, LA, MN, MS, NV, NJ, OH, OK, OR, PA, TN, TX, UT, WA, WI & Puerto Rico, and the countries of Au... [Official source for Dual Articulating Headrest, Velcro P/N P141210813, REF BF753](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0984-2024%22) Nov 16, 2023 FDA device enforcement ### [V. Mueller Universal Bandage Scissors Black Plastic Handles Heavy-Duty, Autoclavable, Overall Length 7 (18 cm)- Intended to cut through tape and bandages Model: SU2014-001](https://isitonrecall.com/recall/fda-device-z-0737-2024-v-mueller-universal-bandage-scissors-black-plastic-handles-heavy-duty-autoclavable-overall-length-7/) Bandage Scissors handle cover component contains an incorrect color masterbatch resin carrier. This may allow a pink dye/residue to appear on the Bandage Scissors and/or sterilization pouches after processing. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for V. Mueller Universal Bandage Scissors Black Plastic Handles Heavy-Duty, Autoclavable, Overall Len...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0737-2024%22) Nov 13, 2023 FDA device enforcement ### [Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS Pass Thru Automated Endoscope Reprocessors Model # Model Description 2-8-001 HU ZERO CHANNEL NO LT 2-8-...](https://isitonrecall.com/recall/fda-device-z-0617-2024-hookup-accessories-used-with-medivators-advantage-plus-and-advantage-plus-pass-thru-automated-endosc/) Identification label on affected hookups could become illegible over time due to the label's ink coming off. This may potentially prevent users from being able to effectively identify the hookup and may ultimately result in postponement of patient procedures. Class II Reported ongoing Distribution: Domestic distribution nationwide. Foreign distribution to Australia Canada China Hong Kong Italy Malaysia Netherlands New Zealand Singapore Thailand [Official source for Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS Pass Thru Automated End...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0617-2024%22) Apr 10, 2023 FDA device enforcement ### [Reliance Vision Multi-Chamber Washer/Disinfector, Reference Number FH83062](https://isitonrecall.com/recall/fda-device-z-1595-2023-reliance-vision-multi-chamber-washer-disinfector-reference-number-fh83062/) In the remote occurrence in which the electrical contactor component present in the drying chambers of the Reliance Vision Multi-Chamber Washer/Disinfector malfunctions, the heating elements in the drying chamber could overheat, eventually resulting in smok... Class II Reported ongoing Distribution: Worldwide Distribution: US (Nationwide) and OUS (Foreign) to countries of: China, Lithuania, Saudi Arabia, Korea, Republic of, Canada, Taiwan, United Kingdom, Spain, Australia, ... [Official source for Reliance Vision Multi-Chamber Washer/Disinfector, Reference Number FH83062](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1595-2023%22) Mar 17, 2023 FDA device enforcement ### [Steris Lighting and Visualization Systems, Sterile Light Handle Cover (LB53)- Surgical light handle covers, including disposable surgical light handle covers are designed to fit...](https://isitonrecall.com/recall/fda-device-z-1475-2023-steris-lighting-and-visualization-systems-sterile-light-handle-cover-lb53-surgical-light-handle-cove/) Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an injury to the patient Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including Puerto Rico and the countries of Canada, Australia. [Official source for Steris Lighting and Visualization Systems, Sterile Light Handle Cover (LB53)- Surgical light hand...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1475-2023%22) Mar 17, 2023 FDA device enforcement ### [Steris Lighting and Visualization Systems, Sterile Light handle Cover LB44 -Sterilizable consumables (disposable, single use) used to drape the lighthandle of STERIS surgical li...](https://isitonrecall.com/recall/fda-device-z-1476-2023-steris-lighting-and-visualization-systems-sterile-light-handle-cover-lb44-sterilizable-consumables-d/) Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an injury to the patient Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including Puerto Rico and the countries of Canada, Australia. [Official source for Steris Lighting and Visualization Systems, Sterile Light handle Cover LB44 -Sterilizable consumab...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1476-2023%22) Dec 12, 2022 FDA device enforcement ### [VERIFY Dual Species Self-Contained Biological Indicators, 50 per box Item Number: S3060 Intended for use in installation testing and routine monitoring of steam and ethylene oxi...](https://isitonrecall.com/recall/fda-device-z-0778-2023-verify-dual-species-self-contained-biological-indicators-50-per-box-item-number-s3060-intended-for-u/) Biological indicator (BI) used to promote growth of the G. stearothermophilus and B. atrophaeus spores was inconsistent in promoting growth throughout lot , some BIs within the lot performed as intended while others did not. When used to monitor steam and e... Class II Reported ongoing Distribution: Nationwide Foreign: AE AT CA CO ES FI GU IN IT JP MX SG TH TW ZA [Official source for VERIFY Dual Species Self-Contained Biological Indicators, 50 per box Item Number: S3060 Intended ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0778-2023%22) ## Reasons in these listed records - There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads. - The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. - Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users). - The DFPM yoke assembly ("yoke assembly") may detach from the spring arm. Should the yoke assembly detach from the spring arm, the yoke assembly would not be expected to fully detach but rather hang from the wiring within the yoke assembly. These examples come from this result page and are not a ranking of every recall reason. ## Checking Steris Corporation ### Is there a recall on steris corporation right now? This archive contains 28 records, including 23 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Steris Corporation](https://isitonrecall.com/check/?q=Steris%20Corporation) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)