Device recall
Z-1344-2019: MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient…
FDA device recall · Class II · Compass Health Brands (Corporate Office)
Key facts
| Recall number (Z-number) | Z-1344-2019 |
|---|---|
| Recall event | 82629 |
| Product | MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient, Model #6103M-S |
| Product code | JOW |
| Recalling firm | Compass Health Brands (Corporate Office) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 26, 2020 |
| 510(k) numbers | K974393 |
| FEI number | 3012316249 |
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