--- title: "Medtronic Navigation, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Medtronic Navigation, 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/medtronic-navigation-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Medtronic Navigation, Inc. recall records **13** reported ongoing 13 records in this archive. Latest source date Dec 4, 2024. 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 Dec 4, 2024 FDA device enforcement ### [Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 The Sterile Percutaneous Reference Pin Set is intended to be used...](https://isitonrecall.com/recall/fda-device-z-1022-2025-medtronic-pin-100mm-sterile-percutaneous-ref-9733235-medtronic-pin-150mm-sterile-percutaneous-ref-97/) Due to an increase in complaint that the percutaneous reference pin would not fit into the patient reference frame or percutaneous pin adapter. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, N... [Official source for Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1022-2025%22) Aug 22, 2024 FDA device enforcement ### [StealthStation S8 App versions 1.3.0 and 1.3.2, (Model # 9735762) The StealthStation System, with StealthStation Spine software, is intended as an aid for precisely locating ana...](https://isitonrecall.com/recall/fda-device-z-0050-2025-stealthstation-s8-app-versions-1-3-0-and-1-3-2-model-9735762-the-stealthstation-system-with-stealths/) Due to two software anomalies that can occur within a spine procedure. Two issues are: 1. Navigation Orientation - when lateral orientation radiographic images are taken, information may appear flipped when utilizing the system (180 degree flipped). 2. Pop-... Class II Reported ongoing Distribution: Worldwide - U.S Nationwide distribution including in the states of AK, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NH, NM, NV, NY, OH, OK... [Official source for StealthStation S8 App versions 1.3.0 and 1.3.2, (Model # 9735762) The StealthStation System, with...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0050-2025%22) Mar 26, 2024 FDA device enforcement ### [Stealth S8 Clinical Software Application, REF: 9735762, CE0344, Rx Only. Used in the StealthStation System as an aid for locating anatomical structures in either open or percuta...](https://isitonrecall.com/recall/fda-device-z-1776-2024-stealth-s8-clinical-software-application-ref-9735762-ce0344-rx-only-used-in-the-stealthstation-syste/) Due to a software issue, there is the potential for a missing digit, letter, or decimal in either the "distance to target" or "tip stop point" display during navigation. Class I Reported ongoing Distribution: Worldwide distribution. US nationwide including Puerto Rico, Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Brazil, Bulgaria, Canada, Canary Islands, Chile, China,... [Official source for Stealth S8 Clinical Software Application, REF: 9735762, CE0344, Rx Only. Used in the StealthStati...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1776-2024%22) Nov 28, 2023 FDA device enforcement ### [Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS](https://isitonrecall.com/recall/fda-device-z-0698-2024-medtronic-ref-9733235-pin-100mm-sterile-percutaneous/) Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit into tap cap, or too tight to remove. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AK, AL, AZ, CA and the countries of Armenia, Australia, Austria, Belgium, Canada, China, Denmark, Finland, France, German... [Official source for Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0698-2024%22) Nov 28, 2023 FDA device enforcement ### [Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS](https://isitonrecall.com/recall/fda-device-z-0699-2024-medtronic-ref-9733236-pin-150mm-sterile-percutaneous/) Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit into tap cap, or too tight to remove. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AK, AL, AZ, CA and the countries of Armenia, Australia, Austria, Belgium, Canada, China, Denmark, Finland, France, German... [Official source for Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0699-2024%22) Sep 27, 2023 FDA device enforcement ### [StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation Cranial software, is intended as an aid for locating anatomical...](https://isitonrecall.com/recall/fda-device-z-0188-2024-stealthstation-s8-application-version-2-0-and-2-0-1-part-9735762-the-stealthstation-system-with-stea/) Due to a software anomaly which potentially could result in the surgical planning data shifting to an unintended location. Class I Reported ongoing Distribution: Worldwide Distribution: U.S. (nationwide): AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV... [Official source for StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, wit...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0188-2024%22) Apr 11, 2023 FDA device enforcement ### [StealthStation Cranial Software, Models: 9735585, 9735586 (kit), 9735587 (kit), used with StealthStation S7/i7 systems](https://isitonrecall.com/recall/fda-device-z-1630-2023-stealthstation-cranial-software-models-9735585-9735586-kit-9735587-kit-used-with-stealthstation-s7-i/) During non-axial/some axial exams, software anomalies occur during procedures affecting depth gauge graphic displays for cranial biopsy; causing displays to no longer synchronize with other navigational information showing inaccurate values, which may resul... Class I Reported ongoing Distribution: Worldwide Distibution: US (nationwide): OH, IL, CA, MI, FL, LA, OK, WA, AR, NJ, MN, MO, WI, MA, ND, NY, MD, OR, AK, NE, TN, AZ, IN, GA, GU, VA, PA, TX, SD, MT, NV, MS, KY, AL, C... [Official source for StealthStation Cranial Software, Models: 9735585, 9735586 (kit), 9735587 (kit), used with Stealth...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1630-2023%22) Apr 11, 2023 FDA device enforcement ### [StealthStation Cranial Software, Model: 9735585, used with StealthStation S7/i7 systems](https://isitonrecall.com/recall/fda-device-z-1666-2023-stealthstation-cranial-software-model-9735585-used-with-stealthstation-s7-i7-systems/) In nonaxial/some axial exams if surgical plan utilized, Target Guidance selected, tip projection utilized, Navigate Projection enabled, software anomaly may occur during tumor resection/shunt placement/deep brain stimulation, where distance to/past target t... Class I Reported ongoing Distribution: US Distribution: PR. OUS (foreign) distribution: ARGENTINA, AUSTRALIA, AUSTRIA, BAHRAIN, BELGIUM, BOSNIA and HERZEGOVINA, BRAZIL, BULGARIA, CANADA, CANARY ISLANDS, CHILE, Colomb... [Official source for StealthStation Cranial Software, Model: 9735585, used with StealthStation S7/i7 systems](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1666-2023%22) Dec 15, 2022 FDA device enforcement ### [AxiEM" Non-Invasive Patient Tracker](https://isitonrecall.com/recall/fda-device-z-1039-2023-axiem-non-invasive-patient-tracker/) Due to increasing complaint trend for the Non-Invasive Patient Tracker system where complaints analysis indicates that users are unable to successfully verify their navigation instruments during image-guided surgery. Class II Reported ongoing Distribution: Worldwide - U.S. distribution including in the states of AL, AR, AZ, CA, CO, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NV, NY, OH, ... [Official source for AxiEM" Non-Invasive Patient Tracker](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1039-2023%22) Dec 8, 2022 FDA device enforcement ### [RadiaLux Lighted Retractor (Pink), REF: 50-101-1](https://isitonrecall.com/recall/fda-device-z-0953-2023-radialux-lighted-retractor-pink-ref-50-101-1/) Defect in sterile pouch seal, incomplete seal, of lighted Retractors, increases the risk of contamination, which can lead to post-operative infection. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of OH, CA, FL, NJ, NY, MN, IN, VA, WA, MS, SC, MO, GA, PA, KS, TN, LA, TX, ME, MA, AL, NC, MD, NH, IL, AZ, MI, NV, MT, OK, SD,... [Official source for RadiaLux Lighted Retractor (Pink), REF: 50-101-1](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0953-2023%22) Oct 14, 2022 FDA device enforcement ### [Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER 10MM TIP product. Used to necrotize or coagulate soft tissue by physicians in minimally invasive surgica...](https://isitonrecall.com/recall/fda-device-z-0244-2023-visualase-cooled-laser-applicator-system-vclas-9735560-4mm-core-fiber-10mm-tip-product-used-to-necro/) Due to a defect in the outer pouch sterile seal Class II Reported ongoing Distribution: U.S. Nationwide distribution including in the states AZ, CA, CO, DC, FL, IL, KY, MA, MD, ME, MI, MN, MO, NH, NJ, NY, OH, PA, RI, TX, VA, WA, and WV. [Official source for Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER 10MM TIP product. Used t...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0244-2023%22) Nov 11, 2021 FDA device enforcement ### [Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial, Model: 9733763, and StealthStation Cranial, Model: 9735585](https://isitonrecall.com/recall/fda-device-z-0383-2022-stealthstation-system-w-stealthstation-cranial-software-3-1-1-3-1-2-3-1-or-synergycranial-software-s/) Cranial biopsy procedure software can enter a state where the biopsy depth gauge is no longer synchronized with the rest of the navigational information on the screen and may display an incorrect position of the biopsy needle, which may result in prolonged ... Class I Reported ongoing Distribution: US: MN, FL, MD, IL, AK, NE, NH, PA, ND, AR, CA, WI, NJ, GA, SD, AZ, KY, AL, MS, MO, TX, MI, MT, OH, NY, VA, MA, CT, TN, WV, WA, NC, CO, NV, ME, LA, DE, NM, IN, UT, DC, OR, SC, O... [Official source for Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Softw...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0383-2022%22) Nov 9, 2021 FDA device enforcement ### [Stealth Autoguide Tracker, Model: 28248, which is an instrument in the Stealth Autoguide Basic Instrument Kit, Mode: 9736188, and the Bundle Autoguide Reg Kit.](https://isitonrecall.com/recall/fda-device-z-0417-2022-stealth-autoguide-tracker-model-28248-which-is-an-instrument-in-the-stealth-autoguide-basic-instrume/) A tracker that holds and guides neurosurgical surgical instruments may be subject to separation/weld failure, where the tracker connects to the instrument tube. If a weld separation occurs and a navigation inaccuracy is experienced, it may result in prolong... Class II Reported ongoing Distribution: US: FL, NE, CA, MN, TX, OH, IL, AZ, KS, KY, OR, OK, WA, NV, MO, IN, MI, UT, MS, VA, SC. OUS: Canada, Sweden, Italy, France, Germany, Spain, Czech Republic, United Kingdom, India... [Official source for Stealth Autoguide Tracker, Model: 28248, which is an instrument in the Stealth Autoguide Basic In...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0417-2022%22) ## Reasons in these listed records - Due to an increase in complaint that the percutaneous reference pin would not fit into the patient reference frame or percutaneous pin adapter. - Due to two software anomalies that can occur within a spine procedure. Two issues are: 1. Navigation Orientation - when lateral orientation radiographic images are taken, information may appear flipped when utilizing the system (180 degree flipped). 2. Pop-up Message - when us... - Due to a software issue, there is the potential for a missing digit, letter, or decimal in either the "distance to target" or "tip stop point" display during navigation. - Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit into tap cap, or too tight to remove. These examples come from this result page and are not a ranking of every recall reason. ## Checking Medtronic Navigation, Inc. ### Is there a recall on medtronic navigation, inc. right now? This archive contains 13 records, including 13 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 Medtronic Navigation, Inc.](https://isitonrecall.com/check/?q=Medtronic%20Navigation%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)