Device recall
Z-2270-2012: Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry
FDA device recall · Class II · Sunquest Information Systems, Inc.
Key facts
| Recall number (Z-number) | Z-2270-2012 |
|---|---|
| Recall event | 62708 |
| Product | Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry |
| Product code | JQP |
| Recalling firm | Sunquest Information Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 27, 2012 |
| 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