Every recall we track for NuVasive Specialized Orthopedics, Inc. — 11 in all — plus the complaints and injury reports the public filed about them.
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.
NuVasive recalls MAGEC 2 Rod spinal braces due to potential sterile packaging failure that could compromise device sterility during use.
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.
NuVasive recalls PRECICE limb lengthening system end caps and screws manufactured between April 2015 and February 2021 that are not indicated for use in individuals under 18 years old due to incomplete biological assessments.
Nuvasive recalls Precice Bone Transport devices for limb lengthening and fracture fixation due to reported pain and bony abnormalities at the telescoping nail segments interface. All affected models are listed in the recall notice.
NuVasive recalls Freedom end caps for PRECICE limb lengthening systems due to lack of biological assessments for patients under 18. Affected items were sold from April 2015 to February 2021.
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.
Nuvasive recalls PRECICE STRYDE devices for limb lengthening and fracture fixation due to reported pain and bony abnormalities at the telescoping nail segments interface. All affected models are listed in the recall notice.
Nuvasive recalls PRECICE plates for limb lengthening and fracture fixation due to reported pain and bony abnormalities at the interface between telescoping nail segments.
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.
NuVasive recalls MAGEC 1 System implants made before March 26, 2015 due to risk of internal component fractures after surgery.
