Device recall
Z-0203-2019: IM Abbott Alinity ci-series (abdicqii) accessory driver v8.00.0001 software…
FDA device recall · Class II · Data Innovations, LLC
Key facts
| Recall number (Z-number) | Z-0203-2019 |
|---|---|
| Recall event | 81005 |
| Product | IM Abbott Alinity ci-series (abdicqii) accessory driver v8.00.0001 software product that can receive information from a hospital computer system (also called a Laboratory Information System [LIS]). |
| Product code | JQP |
| Recalling firm | Data Innovations, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2019 |
| FEI number | 3001451449 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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