NuVasive recalls
NuVasive has 36 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 15 Feb 2023. 3 are still ongoing.
Total recalls36since 2012
Last 12 months0reported
Class I00% of total
Ongoing3latest 15 Feb 2023
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 35 97%Class III 1 3%
Why nuvasive is recalled
Product types
By year
Ongoing nuvasive recalls
3 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS III | MD Pulse III Multimodality System recalled by NuVasive | NuVasive | Device Malfunction | Nationwide |
| Device | CLASS II | X-core 2 Ti Core, Static recalled by NuVasive | NuVasive | Other | Nationwide |
| Device | CLASS II | Description/Part: Simplify Disc Size 1, Ht 5/SM recalled by NuVasive | NuVasive | Lead & Heavy Metals | 10 states |
All nuvasive recalls, newest first
36 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.