NuVasive Specialized Orthopedics, Inc. recalls
Every recall we track for NuVasive Specialized Orthopedics, Inc. — 11 in all, from 2019–2024 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from NuVasive Specialized Orthopedics, Inc. peaked in 2021 (7); 11 since 2017.
All FDA recall records for NuVasive Specialized Orthopedics, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 0 | 0 | 1 |
| 2021 | 0 | 0 | 7 | 0 | 7 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 1 | 1 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled NuVasive Specialized Orthopedics, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All NuVasive Specialized Orthopedics, Inc. recalls
7 shown- UnratedMedical device
NuVasive Specialized Orthopedics, Inc. recalls Precice Max REF: PM10.0-80B265 PRECICE MAX Antegrade Femur Piriformis Straight 10.0mm x 265mm PM10.0-80B280 PRECICE MAX
NuVasive recalls specific Precice Max orthopedic devices due to potential design and documentation issues affecting validation. Affected models include various sizes for femur and tibia fractures.
NuVasiveSep 30, 2024 - Lower riskMedical device
NuVasive Specialized Orthopedics, Inc. recalls NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used to brace the spine during growth to minimize the progression of
NuVasive recalls MAGEC 2 Rod spinal braces due to potential sterile packaging failure that could compromise device sterility during use.
NuVasiveNov 1, 2022 - Lower riskMedical device
NuVasive Specialized Orthopedics, Inc. recalls NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product
NuVasive recalls Precice Intramedullary Limb Lengthening systems for age, weight, and device count restrictions. Updated instructions clarify patients must be 18+, weigh at least 50 lbs, and no more than two devices can be implanted.
NuVasiveOct 29, 2021 - Lower riskMedical device
Nuvasive Specialized Orthopedics Inc recalls NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail System/PRECICE Unyte-Humerus Orthopedic trauma
NuVasive recalls PRECICE Unyte Humerus and Tibia trauma nail systems due to insufficient biological assessments for patients under 18. These devices are not indicated for use in individuals under 18 years old.
NuVasiveFeb 12, 2021 - Lower riskMedical device
Nuvasive Specialized Orthopedics Inc recalls PRECICE PLATE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis,
Nuvasive recalls PRECICE plates for limb lengthening and fracture fixation due to reported pain and bony abnormalities at the interface between telescoping nail segments.
NuvasiveFeb 12, 2021 - Use cautionMedical device
Nuvasive Specialized Orthopedics Inc recalls NUVASIVE SPECIALIZED ORTHOPEDICS, INC. Precice Bone Transport Antegrade Femur Trochanter 10 Degree Bend Component of
Recall of specific NuVasive Precice Bone Transport components due to risk of bone plug detaching during removal. Affected items include certain femur and tibia components with specific lot numbers.
NuVasiveJul 24, 2020 - Lower riskMedical device
NuVasive Specialized Orthopedics, Inc. recalls MAGEC 1 System
NuVasive recalls MAGEC 1 System implants made before March 26, 2015 due to risk of internal component fractures after surgery.
NuVasiveJun 25, 2019
NuVasive Specialized Orthopedics, Inc. recall questions
How many recalls has NuVasive Specialized Orthopedics, Inc. had?
11 recalls from NuVasive Specialized Orthopedics, Inc. are on record with U.S. safety agencies, from 2019–2024.
What is the most recent NuVasive Specialized Orthopedics, Inc. recall?
NuVasive Specialized Orthopedics, Inc. recalls Precice Max REF: PM10.0-80B265 PRECICE MAX Antegrade Femur Piriformis Straight 10.0mm x 265mm PM10.0-80B280 PRECICE MAX, dated Sep 30, 2024. Every NuVasive Specialized Orthopedics, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled NuVasive Specialized Orthopedics, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new NuVasive Specialized Orthopedics, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.