Device recall
Z-2775-2016: Endura MD Mass Spectrometer u using software versions Endura MD Software 1.0 and…
FDA device recall · Class II · Thermo Finnigan LLC
Key facts
| Recall number (Z-number) | Z-2775-2016 |
|---|---|
| Recall event | 74837 |
| Product | Endura MD Mass Spectrometer u using software versions Endura MD Software 1.0 and 1.0 SP1. In vitro diagnostic medical device used to identify and quantify inorganic and organic compounds in the human body. Chemistry: In vitro diagnostic medical device used to identify and quantify inorganic and… |
| Product code | DOP |
| Recalling firm | Thermo Finnigan LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 21, 2017 |
| FEI number | 3003809634 |
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