Device recall
Z-0207-2009: Sunquest Laboratory versions 5.3, 5.4, 6.1, 6.2 and 6.3. Sunquest Laboratory…
FDA device recall · Class II · Sunquest Information Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0207-2009 |
|---|---|
| Recall event | 48174 |
| Product | Sunquest Laboratory versions 5.3, 5.4, 6.1, 6.2 and 6.3. Sunquest Laboratory Information System is comprised of several modules which are involved in aspects such as blood banking, collection management, specimen tracking, and use with microbiology and molecular diagnostics. Key capabilities… |
| Product code | JQP |
| Recalling firm | Sunquest Information Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 5, 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