Corin recalls
Corin has 21 recalls on record with the FDA and USDA, the earliest in 2021 and the latest reported on 8 Nov 2023. 5 are still ongoing. The most frequent reason is sterility.
Total recalls21since 2021
Last 12 months0reported
Class I00% of total
Ongoing5latest 8 Nov 2023
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 21 100%Class III 0 0%
Why corin is recalled
Product types
By year
Ongoing corin recalls
5 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Unity CR Femur Right, Size recalled by Corin | Corin | Labeling Errors | IL, MI, TX |
| Device | CLASS II | Unity Total Knee System recalled by Corin | Corin | Labeling Errors | IL, MI, TX |
| Device | CLASS II | Biolox Delta Mod Head, Ex Long + recalled by Corin | Corin | Other | Nationwide |
| Device | CLASS II | Biolox Delta Mod Head Ex Long + recalled by Corin | Corin | Other | Nationwide |
| Device | CLASS II | Metafix Hip Stem, Size 3, Standard, 135 degrees recalled by Corin | Corin | Labeling Errors | Nationwide |
All corin recalls, newest first
21 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Unity CR Femur Right, Size recalled by Corin | Corin | Labeling Errors | IL, MI, TX |
| Device | CLASS II | Unity Total Knee System recalled by Corin | Corin | Labeling Errors | IL, MI, TX |
| Device | CLASS II | Biolox Delta Mod Head, Ex Long + recalled by Corin | Corin | Other | Nationwide |
| Device | CLASS II | Biolox Delta Mod Head Ex Long + recalled by Corin | Corin | Other | Nationwide |
| Device | CLASS II | Unity Total Knee System recalled by Corin | Corin | Sterility | Nationwide |
| Device | CLASS II | TaperFit Stem, Size 0 Offset recalled by Corin | Corin | Other | NJ |
| Device | CLASS II | Metafix Hip Stem, Size 3, Standard, 135 degrees recalled by Corin | Corin | Labeling Errors | Nationwide |
| Device | CLASS II | Trinity Screw, diameter Length, Cancellous Bone Screw recalled by Corin | Corin | Sterility | Nationwide |
| Device | CLASS II | Trinity Dual Mobility, Size 4, Dual Mobility CoCr Liner recalled | Corin | Sterility | Nationwide |
| Device | CLASS II | Trinity Liner Ecima, diameter Neutral Offset, Taper Size recalled | Corin | Sterility | 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.