Device recall
Z-2717-2016: NOMAD Pro2 Packaged X-Ray System, Part Number 08500021; NOMAD Pro2 Packaged…
FDA device recall · Class II · Aribex Inc
Key facts
| Recall number (Z-number) | Z-2717-2016 |
|---|---|
| Recall event | 74975 |
| Product | NOMAD Pro2 Packaged X-Ray System, Part Number 08500021; NOMAD Pro2 Packaged X-Ray System Black, Part Number 08500022; NOMAD Pro2 Vet Packaged X-Ray System, Part Number 08500023; NOMAD Pro2 Vet Packaged X-Ray System Black, Part Number 08500024; NOMAD Pro2 Packaged X-Ray System, GBL, Part Number… |
| Product code | EHD |
| Recalling firm | Aribex Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 26, 2017 |
| 510(k) numbers | K081664 |
| FEI number | 1017522 |
At a glance
- 1–9 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