Device recall
Z-0183-2012: Pulstar(R) DVT PREVENTION SYSTEM, Anti-Embolism Wrap System, albahealth(R), A…
FDA device recall · Class II · Albahealth LLC
Key facts
| Recall number (Z-number) | Z-0183-2012 |
|---|---|
| Recall event | 60122 |
| Product | Pulstar(R) DVT PREVENTION SYSTEM, Anti-Embolism Wrap System, albahealth(R), A Subsidiary of Encompass Group, LLC. Prevention of DVT. |
| Product code | JOW |
| Recalling firm | Albahealth LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 30, 2012 |
| 510(k) numbers | K961405 |
| FEI number | 1043612 |
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