Medacta U recalls
Medacta U has 3 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 25 Nov 2015. The most frequent reason is packaging defects.
Total recalls3since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 25 Nov 2015
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why medacta u is recalled
Product types
By year
All medacta u recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | GMK Hinge knee prosthesis recalled by Medacta U | Medacta U | Packaging Defects | IL, OH, UT |
| Device | CLASS II | The MectaLIF Oblique Handle recalled by Medacta U | Medacta U | Other | Nationwide |
| Device | CLASS II | GMK Intramedullary Extension Rod is a rod to obtain correct recalled | Medacta U | Device Malfunction | Nationwide |
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.