Device recall
Z-0214-2009: Sunquest Laboratory System. Software Version: Sunquest Laboratory v5.4.2, v6.1…
FDA device recall · Class II · Sunquest Information Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0214-2009 |
|---|---|
| Recall event | 49136 |
| Product | Sunquest Laboratory System. Software Version: Sunquest Laboratory v5.4.2, v6.1, v6.2 and v6.3. The system is marketed as an automated solution for managing laboratory processes including: 1) Patient registration, 2) Order entry and order modification, 3) Specimen collection, verification… |
| Product code | JQP |
| Recalling firm | Sunquest Information Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 28, 2011 |
| FEI number | 1000306472 |
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