Device recall
Z-0069-2022: CardioQuip, Modular Cooler-Heater 1000(i), Refrigeration Module, Model…
FDA device recall · Class II · CardioQuip, LLC
Key facts
| Recall number (Z-number) | Z-0069-2022 |
|---|---|
| Recall event | 88621 |
| Product | CardioQuip, Modular Cooler-Heater 1000(i), Refrigeration Module, Model: MCH-10RMS, UDI: (01)00860000846127 used with heat exchange devices. |
| Product code | DWC |
| Recalling firm | CardioQuip, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K102147 |
| FEI number | 3007899424 |
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