--- title: "IMRIS Imaging Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search IMRIS Imaging Inc recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/imris-imaging-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # IMRIS Imaging Inc recall records **3** reported ongoing 3 records in this archive. Latest source date Aug 6, 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 Aug 6, 2026 FDA device enforcement ### [ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Number 113821-600 and the ORT200 50/60Hz Covered Table Assy V2 Part Number 114148-000](https://isitonrecall.com/recall/fda-device-z-3033-2026-ort200-operating-room-table-including-the-ort200-covered-table-assembly-reconditioned-part-number-11/) The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may pose a risk of injury to the patient if unintended rotational movement o... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Canada, China, Japan, Sweden. [Official source for ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Nu...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3033-2026%22) Aug 6, 2026 FDA device enforcement ### [ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600](https://isitonrecall.com/recall/fda-device-z-3034-2026-ort300-operating-room-table-ort300-modular-table-main-unit-assy-part-numbers-114093-000-and-114093-6/) The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may pose a risk of injury to the patient if unintended rotational movement o... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Canada, China, Japan, Sweden. [Official source for ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3034-2026%22) Dec 8, 2025 FDA device enforcement ### [Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number: 119695-000, 119629-000, 119630-000, 113803-000, 113803-600, 113802-000, 113802-600 Software Ve...](https://isitonrecall.com/recall/fda-device-z-1034-2026-brand-name-hfd100-product-name-head-fixation-device-hfd100-model-catalog-number-119695-000-119629-00/) Torque screw may crack or separate. If used, an affected screw could lead to inadequate head stabilization, compromised surgical precision, procedural delays, requirement for alternate head fixation methods, and risk of patient injury. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Sweden, Switzerland, Japan, Australia, Qatar, and China. [Official source for Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number: 119695-000, 11...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1034-2026%22) ## Reasons in these listed records - The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may pose a risk of injury to the patient if unintended rotational movement occurs during a proce... - Torque screw may crack or separate. If used, an affected screw could lead to inadequate head stabilization, compromised surgical precision, procedural delays, requirement for alternate head fixation methods, and risk of patient injury. These examples come from this result page and are not a ranking of every recall reason. ## Checking IMRIS Imaging Inc ### Is there a recall on imris imaging inc right now? This archive contains 3 records, including 3 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 IMRIS Imaging Inc](https://isitonrecall.com/check/?q=IMRIS%20Imaging%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)