Device recall
Z-1365-2013: MEDITECH Bi-Directional interactive Communication Analyzer Interface; Integrates…
FDA device recall · Class II · Medical Information Technology, Inc.
Key facts
| Recall number (Z-number) | Z-1365-2013 |
|---|---|
| Recall event | 65158 |
| Product | MEDITECH Bi-Directional interactive Communication Analyzer Interface; Integrates with MEDITECH's Laboratory Information System (LIS) with Other Vendor systems to manage the transfer of patient results and demographic information. |
| Product code | OUG |
| Recalling firm | Medical Information Technology, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 1, 2014 |
| FEI number | 1000120736 |
At a glance
- None 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