Device recall
Z-0856-2015: Lite DM (Lite Data Manager) Software Version(s): Versions 2.0.0.19 and lower…
FDA device recall · Class II · Horiba Instruments Inc
Key facts
| Recall number (Z-number) | Z-0856-2015 |
|---|---|
| Recall event | 69847 |
| Product | Lite DM (Lite Data Manager) Software Version(s): Versions 2.0.0.19 and lower Product Model #: D00A00224D The Lite DM (Lite Data Manager) is a software application developed by HORIBA Medical intended to receive, store, and manage Startup, Patient, and Quality Control (QC) results from an ABX Micros… |
| Product code | OUG |
| Recalling firm | Horiba Instruments Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 22, 2015 |
| FEI number | 3002698356 |
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