Device recall
Z-2937-2020: SINGLES Carbide US-No. FG556; UDI +E0HM26000313140091; STERILE R; Size 009…
FDA device recall · Class II · Hager & Meisinger Gmbh
Key facts
| Recall number (Z-number) | Z-2937-2020 |
|---|---|
| Recall event | 86147 |
| Product | SINGLES Carbide US-No. FG556; UDI +E0HM26000313140091; STERILE R; Size 009, Length 3.8; 2025-03-18 - Product Usage: Cutting of hard structures in the mouth, such as teeth or bone, it is also intended to cut hard metals, plastics, porcelains, and similar materials intended for use in the fabrication… |
| Product code | EJL |
| Recalling firm | Hager & Meisinger Gmbh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 24, 2022 |
| FEI number | 3004169071 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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