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NuVasive Specialized Orthopedics, Inc. recalls MAGEC 1 System
Recalled February 2, 2022 · FDA recall Z-0528-2022 · NuVasive Specialized Orthopedics
Hazard
Safety Alert to all surgeons informing them of post-implantation fractures of an internal metallic component for device manufactured prior to March 26, 2015. · FDA Class II
Units
3,056 devices
Sold at
Worldwide
Description
Safety Alert to all surgeons informing them of post-implantation fractures of an internal metallic component for device manufactured prior to March 26, 2015.
Product
MAGEC 1 System
Manufacturer(s)
NuVasive Specialized Orthopedics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →