Device recall
Z-2849-2016: TriMed Semi-Tubular Plate, 10-Hole, Model No. SMTP-10 Contoured plate with…
FDA device recall · Class II · Trimed Inc
Key facts
| Recall number (Z-number) | Z-2849-2016 |
|---|---|
| Recall event | 75080 |
| Product | TriMed Semi-Tubular Plate, 10-Hole, Model No. SMTP-10 Contoured plate with offset screw holes. The plate is 103 mm in length, 1.3 mm thick and 9.6 mm wide. The part is made of surgical steel conformance with ASTM F138 or F139. The plate is used to fixation of long bone fractures. The TriMed Bone… |
| Product code | HRS |
| Recalling firm | Trimed Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 1, 2016 |
| 510(k) numbers | K060041 |
| FEI number | 3001236812 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database