Device recall
Z-0402-2019: DT Medical -Hintermann Series H3 Poly Inlay, Size 3 5mm Part Number: 300305…
FDA device recall · Class II · DT MedTech, LLC
Key facts
| Recall number (Z-number) | Z-0402-2019 |
|---|---|
| Recall event | 81293 |
| Product | DT Medical -Hintermann Series H3 Poly Inlay, Size 3 5mm Part Number: 300305 components are prostheses for a mobile bearing ankle joint. |
| Product code | NTG |
| Recalling firm | DT MedTech, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 5, 2019 |
| FEI number | 3012104767 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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