Device recall
Z-1924-2011: Quest MPS and MPS 2 Consoles, Quest Medical, Inc., An Atrion company. Single…
FDA device recall · Class III · Quest Medical, Inc
Key facts
| Recall number (Z-number) | Z-1924-2011 |
|---|---|
| Recall event | 57141 |
| Product | Quest MPS and MPS 2 Consoles, Quest Medical, Inc., An Atrion company. Single software controlled device that incorporates a pump, a heater/cooler, temperature monitoring, pressure monitoring, a heat exchanger, an arrest agent pump and an additive pump. The MPS console is used with the MPS sterile… |
| Product code | DTR |
| Recalling firm | Quest Medical, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 26, 2011 |
| 510(k) numbers | K041979, K953838 |
| FEI number | 3001665800 |
At a glance
- 1–9 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