--- title: "NuVasive Specialized Orthopedics, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search NuVasive Specialized Orthopedics, 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/nuvasive-specialized-orthopedics-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # NuVasive Specialized Orthopedics, Inc. recall records **3** reported ongoing 3 records in this archive. Latest source date Sep 30, 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 Sep 30, 2024 FDA device enforcement ### [Precice Max REF: PM10.0-80B265 PRECICE MAX Antegrade Femur Piriformis Straight 10.0mm x 265mm PM10.0-80B280 PRECICE MAX Antegrade Femur Piriformis Straight 10.0mm x 280mm PM10.0...](https://isitonrecall.com/recall/fda-device-z-0500-2025-precice-max-ref-pm10-0-80b265-precice-max-antegrade-femur-piriformis-straight-10-0mm-x-265mm-pm10-0/) Due to potential issues with design, manufacturing and documentation issues related to the validation of the affected products/devices. Class II Reported ongoing Distribution: U.S distribution to states of: FL and NV. [Official source for Precice Max REF: PM10.0-80B265 PRECICE MAX Antegrade Femur Piriformis Straight 10.0mm x 265mm PM1...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0500-2025%22) Nov 1, 2022 FDA device enforcement ### [NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used to brace the spine during growth to minimize the progression of scoliosis. REF Model Numbers/NSO Item #/Product Description ...](https://isitonrecall.com/recall/fda-device-z-0559-2023-nuvasive-magec-magec-2-rod-the-magec-system-is-used-to-brace-the-spine-during-growth-to-minimize-the/) During accelerated shelf-life extension studies it was noted that the final packaging was experiencing a potential of failure of the sterile packaging barrier which could result in a hazardous situation where the device is no longer sterile. Class II Reported ongoing Distribution: Distribution US nationwide including Puerto Rico; Chile, Israel, Jordan, New Zealand, Singapore, Sweden, Thailand, and United Arab Emirates. [Official source for NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used to brace the spine during growth to minimize...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0559-2023%22) Oct 29, 2021 FDA device enforcement ### [NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product Description: CPA1-000 PA0382-001 End Cap CPA2-000 PA1051-000 PACKAGE...](https://isitonrecall.com/recall/fda-device-z-0319-2022-nuvasive-precice-intramedullary-limb-lengthening-imll-and-short-system-model-number-item-number-prod/) The Instructions for Use have been updated to include: (1) Clarification that the device is intended for use only in patients 18 years and older, (2) That patients should weigh 50 lbs. or more while undergoing treatment, and (3) That no more than two device... Class II Reported ongoing Distribution: U.S.: AK, AL, AR, AZ, CA, CO, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, Puerto Rico, RI, SC, TN... [Official source for NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Num...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0319-2022%22) ## Reasons in these listed records - Due to potential issues with design, manufacturing and documentation issues related to the validation of the affected products/devices. - During accelerated shelf-life extension studies it was noted that the final packaging was experiencing a potential of failure of the sterile packaging barrier which could result in a hazardous situation where the device is no longer sterile. - The Instructions for Use have been updated to include: (1) Clarification that the device is intended for use only in patients 18 years and older, (2) That patients should weigh 50 lbs. or more while undergoing treatment, and (3) That no more than two devices should be implante... These examples come from this result page and are not a ranking of every recall reason. ## Checking NuVasive Specialized Orthopedics, Inc. ### Is there a recall on nuvasive specialized orthopedics, 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 NuVasive Specialized Orthopedics, Inc.](https://isitonrecall.com/check/?q=NuVasive%20Specialized%20Orthopedics%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)