--- title: "Medtronic Xomed, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Medtronic Xomed, 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-xomed-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Medtronic Xomed, Inc. recall records **11** reported ongoing 12 records in this archive. Latest source date Jul 17, 2025. 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 Jul 17, 2025 FDA device enforcement ### [IPC Powerease System REF 2300000 UDI-DI: 00613994448705 00643169406834. The IPC POWEREASE System is indicated for drilling, tapping, and driving screws and working end attachmen...](https://isitonrecall.com/recall/fda-device-z-2461-2025-ipc-powerease-system-ref-2300000-udi-di-00613994448705-00643169406834-the-ipc-powerease-system-is-in/) Due to out of the box wobble of the driver. Class II Reported ongoing Distribution: U.S.: AZ, CA, CO, CT, FL, GA, IA, IL, IN, LA, MI, MN, MO, MS, NC, ND, NE, NJ, NV, NY, OH, OR, SC, TN, TX, O.U.S.: Canada, China, Croatia, France, Germany, India, Italy, Japan, J... [Official source for IPC Powerease System REF 2300000 UDI-DI: 00613994448705 00643169406834. The IPC POWEREASE System ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2461-2025%22) Mar 10, 2025 FDA device enforcement ### [NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0, REF: NIM4CM01; CONSOLE NIM4CM01RF NIM 4.0 REFURBISHED, REF: NIM4CM01RF; PATIENT INTERFACE NIM4CPB1 NIM 4.0, REF: NIM...](https://isitonrecall.com/recall/fda-device-z-1623-2025-nim-vital-nerve-monitoring-system-console-nim4cm01-nim-4-0-ref-nim4cm01-console-nim4cm01rf-nim-4-0-r/) Nerve Monitoring System with certain software versions has potential for increased stimulus artifact, which may require troubleshooting, and may lead to procedure delay, extubation, and medical intervention. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of MD, MN, PA, OK, OH, FL, CO, GA, NC, KS, IL, WY, AK, NE, VA, MI, CA, NY, WI, UT, AZ, AR, TX, WA, AL, NJ, SD, MS,... [Official source for NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0, REF: NIM4CM01; CONSOLE NIM4CM01RF NI...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1623-2025%22) Jul 5, 2024 FDA device enforcement ### [Medtronic ENT Ultra Round Steel Cutting Bur, Model Number REF 31313069](https://isitonrecall.com/recall/fda-device-z-3130-2024-medtronic-ent-ultra-round-steel-cutting-bur-model-number-ref-31313069/) Product was distributed past expiration date. Class II Reported ongoing Distribution: International distribution to the country of Canada. [Official source for Medtronic ENT Ultra Round Steel Cutting Bur, Model Number REF 31313069](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3130-2024%22) Jun 24, 2024 FDA device enforcement ### [NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with NIM Vital System versions: v1.0.0, v1.1.1, v1.3.2, v1.4.3. NIM Vital Nerve Integrity Monitor with below...](https://isitonrecall.com/recall/fda-device-z-2409-2024-nim-vital-nerve-monitoring-systems-all-serial-numbers-manufactured-with-nim-vital-system-versions-v1/) Potential for false negative response on the NIM Vital Nerve Monitoring System Class I Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Algeria, Argentina, Armenia, Australia, Austria, Bahrain, Belgium, Bulgaria, Canada, Canary Islands, Cayman Islands, ... [Official source for NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with NIM Vital System versio...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2409-2024%22) Nov 7, 2023 FDA device enforcement ### [NIM TriVantage EMG Endotracheal Tubes, Model (REF) Numbers and sizes: a) 8229706, 6.0MM ID; b) 8229707, 7.0MM ID; c) 8229708, 8.0MM ID; d) 8229736, 6MM ID 3PK; e) 8229737, 7MM I...](https://isitonrecall.com/recall/fda-device-z-0696-2024-nim-trivantage-emg-endotracheal-tubes-model-ref-numbers-and-sizes-a-8229706-6-0mm-id-b-8229707-7-0mm/) Firm received reports of customers experiencing noise from the NIM System, lead-off or high impedance issues, or loss of/intermittent nerve monitoring, Class II Reported ongoing Distribution: Worldwide distribution. [Official source for NIM TriVantage EMG Endotracheal Tubes, Model (REF) Numbers and sizes: a) 8229706, 6.0MM ID; b) 82...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0696-2024%22) May 3, 2022 FDA device enforcement ### [NIM Vital Console 4.0 (P/N: NIM4CM01) NIM with Software version 1.3.2](https://isitonrecall.com/recall/fda-device-z-1223-2022-nim-vital-console-4-0-p-n-nim4cm01-nim-with-software-version-1-3-2/) Software anomaly was identified. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide distribution in the states of TX, CO, NJ and the country of France. [Official source for NIM Vital Console 4.0 (P/N: NIM4CM01) NIM with Software version 1.3.2](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1223-2022%22) May 3, 2022 FDA device enforcement ### [NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version 1.3.2](https://isitonrecall.com/recall/fda-device-z-1224-2022-nim-vital-patient-interface-4-0-p-n-nim4cpb1-nim-with-software-version-1-3-2/) Software anomaly was identified. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide distribution in the states of TX, CO, NJ and the country of France. [Official source for NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version 1.3.2](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1224-2022%22) Apr 29, 2022 FDA device enforcement ### [NIM CONTACT EMG Endotracheal Tube, Part Numbers: a) REF 8229508 b) REF 8229507 c) REF 8229506](https://isitonrecall.com/recall/fda-device-z-1519-2022-nim-contact-emg-endotracheal-tube-part-numbers-a-ref-8229508-b-ref-8229507-c-ref-8229506/) The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes. Class I Reported ongoing Distribution: Worldwide distribution: US (nationwide) and OUS (foreign) countries of: Algeria, Argentina, Australia, Austria, Belgium, Brazil, Canada, Canary Islands, Chile, China, Colombia, ... [Official source for NIM CONTACT EMG Endotracheal Tube, Part Numbers: a) REF 8229508 b) REF 8229507 c) REF 8229506](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1519-2022%22) Apr 29, 2022 FDA device enforcement ### [NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229308 b) REF 8229307 c) REF 8229306](https://isitonrecall.com/recall/fda-device-z-1520-2022-nim-emg-endotracheal-tube-part-numbers-a-ref-8229308-b-ref-8229307-c-ref-8229306/) The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes. Class I Reported ongoing Distribution: Worldwide distribution: US (nationwide) and OUS (foreign) countries of: Algeria, Argentina, Australia, Austria, Belgium, Brazil, Canada, Canary Islands, Chile, China, Colombia, ... [Official source for NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229308 b) REF 8229307 c) REF 8229306](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1520-2022%22) Apr 29, 2022 FDA device enforcement ### [NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J](https://isitonrecall.com/recall/fda-device-z-1521-2022-nim-emg-endotracheal-tube-part-numbers-a-ref-8229307j-b-ref-8229308j-c-ref-8229306j/) The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes. Class I Reported ongoing Distribution: Worldwide distribution: US (nationwide) and OUS (foreign) countries of: Algeria, Argentina, Australia, Austria, Belgium, Brazil, Canada, Canary Islands, Chile, China, Colombia, ... [Official source for NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1521-2022%22) Dec 22, 2021 FDA device enforcement ### [NIM TRIVANTAGE EMG Endotracheal Tube](https://isitonrecall.com/recall/fda-device-z-0743-2022-nim-trivantage-emg-endotracheal-tube/) There is potential for multiple issues due to a manufacturing nonconformity. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Brazil, Canada, Canary Islands, Chile, China, C... [Official source for NIM TRIVANTAGE EMG Endotracheal Tube](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0743-2022%22) Dec 15, 2021 FDA device enforcement ### [Software 1898072 IPC upgrade v 2.7.3.0, IPC System: a) CONSOLE 1898001 IPC, Product Number 1898001; b) CONSOLE IPC REFURB, Product Number EC300RF; c) MASTER CONSOLE EC300 LEGEND...](https://isitonrecall.com/recall/fda-device-z-0961-2022-software-1898072-ipc-upgrade-v-2-7-3-0-ipc-system-a-console-1898001-ipc-product-number-1898001-b-con/) As a result of Medtronic's integrated power console (authentication number: 222ACBZX00018000) being used with software version: v2.7.3.0, it was discovered that there was a defect that resulted in a difference between the set number of rotations and the act... Class II Reported terminated Distribution: International distribution country of Japan. [Official source for Software 1898072 IPC upgrade v 2.7.3.0, IPC System: a) CONSOLE 1898001 IPC, Product Number 189800...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0961-2022%22) ## Reasons in these listed records - Due to out of the box wobble of the driver. - Nerve Monitoring System with certain software versions has potential for increased stimulus artifact, which may require troubleshooting, and may lead to procedure delay, extubation, and medical intervention. - Product was distributed past expiration date. - Potential for false negative response on the NIM Vital Nerve Monitoring System These examples come from this result page and are not a ranking of every recall reason. ## Checking Medtronic Xomed, Inc. ### Is there a recall on medtronic xomed, inc. right now? This archive contains 12 records, including 11 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 Xomed, Inc.](https://isitonrecall.com/check/?q=Medtronic%20Xomed%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)