Device recall
Z-2716-2016: NOMAD Pro Packaged X-Ray System, Part Number 08500009; NOMAD Pro Vet Packaged…
FDA device recall · Class II · Aribex Inc
Key facts
| Recall number (Z-number) | Z-2716-2016 |
|---|---|
| Recall event | 74975 |
| Product | NOMAD Pro Packaged X-Ray System, Part Number 08500009; NOMAD Pro Vet Packaged X-Ray System, Part Number 08500011; NOMAD Pro Packaged X-Ray System - Europe, Part Number 08500013; NOMAD Pro X-Ray System, Remote Config., Part Number 08500017; NOMAD Pro Packaged X-Ray System JP, Part Number 08500019 |
| 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