Device recall
Z-2288-2019: ARIES Extraction Kit; ARIES System; SYNCT, REF 50-10026, UDI # 00840487100073
FDA device recall · Class II · Luminex Corporation
Key facts
| Recall number (Z-number) | Z-2288-2019 |
|---|---|
| Recall event | 83470 |
| Product | ARIES Extraction Kit; ARIES System; SYNCT , REF 50-10026, UDI # 00840487100073 |
| Product code | OOI |
| Recalling firm | Luminex Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K160517 |
| FEI number | 3002524000 |
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