Device recall
Z-2255-2016: Olympus Scientific Solutions Americas Corporation (OSSA) Model: Analytical X-Ray…
FDA device recall · Class II · Olympus Scientific Solutions Americas
Key facts
| Recall number (Z-number) | Z-2255-2016 |
|---|---|
| Recall event | 74593 |
| Product | Olympus Scientific Solutions Americas Corporation (OSSA) Model: Analytical X-Ray System X -Ray Fluorescence. Intended to emit ionizing radiation Delta with models: DC-2000, DC-4000, DC-6000, DI-2000, DP-2000, DP-4000, DP-4050, DP- 6000, DPO-4000, DPO-6000, DS-2000, DS-4000, DS-6000, DS-6500, Delta… |
| Product code | RBY |
| Recalling firm | Olympus Scientific Solutions Americas |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3006241029 |
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