Device recall
Z-2482-2019: HS Hi-R NEO 900 Reference # 657 820 Serial # from 101 Product Usage: A wide…
FDA device recall · Class II · Haag-Streit USA Inc
Key facts
| Recall number (Z-number) | Z-2482-2019 |
|---|---|
| Recall event | 83571 |
| Product | HS Hi-R NEO 900 Reference # 657 820 Serial # from 101 Product Usage: A wide range of surgical interventions are made possible through the modular construction and the diversity of the equipment and accessories. The operating microscope HS Hi-R NEO 900/HS Hi-R NEO 900A/HS Hi-R NEO 900A NIR and HS… |
| Product code | EPT |
| Recalling firm | Haag-Streit USA Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 16, 2020 |
| FEI number | 1000136533 |
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