Home › Nuvasive, Inc. › MAGEC
MAGEC
Nuvasive, Inc. · Model MC2-5070R · UDI-DI 00887517834010
PGN
Prescription
1
510(k) clearances
1,095
Adverse events
4
Recalls
13
Facilities
Description
MAGEC 2 Rod, 5.0mm 70mm Offset
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-04-03 | Globus Medical, Inc. | Devices for the affected lot were not assembled according to product specifications. The distraction rod outer diameter was assembled with a 5.5mm rod versus the required 5.0mm. |
| 2022-11-01 | NuVasive Specialized Orthopedics, Inc. | 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 |
| 2020-02-13 | NuVasive Inc | Post-implantation separation of an actuator end cap component that may expose internal components of the actuator, which could lead to hastened degeneration of the internal compone |
| 2019-06-25 | NuVasive Specialized Orthopedics, Inc. | Safety Alert to all surgeons informing them of post-implantation fractures of an internal metallic component for device manufactured prior to March 26, 2015. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.