TriMed recalls
TriMed has 19 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 22 May 2024. 9 are still ongoing. The most frequent reason is sterility.
Total recalls19since 2016
Last 12 months0reported
Class I00% of total
Ongoing9latest 22 May 2024
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 19 100%Class III 0 0%
Why trimed is recalled
Product types
By year
Ongoing trimed recalls
9 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Threaded IM Nail, TI recalled by TriMed | TriMed | Sterility | Nationwide |
| Device | CLASS II | Threaded IM Nail, TI recalled by TriMed | TriMed | Sterility | Nationwide |
| Device | CLASS II | Volar Bearing Plate recalled by TriMed | TriMed | Other | 5 states |
| Device | CLASS II | RipCord Syndesmosis Button recalled by TriMed | TriMed | Device Malfunction | Nationwide |
| Device | CLASS II | Wrist Hook Dorsal Impactor recalled by TriMed | TriMed | Sterility | Nationwide |
| Device | CLASS II | Hex Driver 2 AO Cannulated recalled by TriMed | TriMed | Sterility | Nationwide |
All trimed recalls, newest first
19 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Threaded IM Nail, TI recalled by TriMed | TriMed | Sterility | Nationwide |
| Device | CLASS II | Threaded IM Nail, TI recalled by TriMed | TriMed | Sterility | Nationwide |
| Device | CLASS II | Volar Bearing Plate recalled by TriMed | TriMed | Other | 5 states |
| Device | CLASS II | RipCord Syndesmosis Button recalled by TriMed | TriMed | Device Malfunction | Nationwide |
| Device | CLASS II | Wrist Hook Dorsal Impactor recalled by TriMed | TriMed | Sterility | Nationwide |
| Device | CLASS II | Olecranon Hook Plate, Lt, 6-Holes recalled by TriMed | TriMed | Sterility | Nationwide |
| Device | CLASS II | Hex Driver 2 AO Cannulated recalled by TriMed | TriMed | Sterility | Nationwide |
| Device | CLASS II | Locking Drill Guide recalled by TriMed | TriMed | Sterility | Nationwide |
| Device | CLASS II | Peg Guide Extender recalled by TriMed | TriMed | Sterility | Nationwide |
| Device | CLASS II | Countersink, HCS recalled by TriMed | TriMed | 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.