Monteris Medical recalls
Monteris Medical has 4 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 28 Mar 2018.
Total recalls4since 2014
Last 12 months0reported
Class I250% of total
Ongoing0latest 28 Mar 2018
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 2 50%Class II 2 50%Class III 0 0%
Why monteris medical is recalled
Product types
By year
All monteris medical recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | Neuroblate System, used for Mri-guided neurosurgical ablation recalled | Monteris Medical | Other | Nationwide |
| Device | CLASS I | NeuroBlate System SideFire Select Directional Laser Probe recalled | Monteris Medical | Sterility | Nationwide |
| Device | CLASS II | SideFire Directional Laser Probe recalled by Monteris Medical | Monteris Medical | Other | 12 states |
| Device | CLASS II | FullFire Diffusing Tip Laser Probe recalled by Monteris Medical | Monteris Medical | Other | 12 states |
About 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.