Device recall
Z-0387-2012: ActiveCare DVT Medical Compression Systems OR Aqiva, IL Intended for use in…
FDA device recall · Class II · Medical Compression Systems
Key facts
| Recall number (Z-number) | Z-0387-2012 |
|---|---|
| Recall event | 59812 |
| Product | ActiveCare DVT Medical Compression Systems OR Aqiva, IL Intended for use in: Preventing deep Vein Thrombosis; Enhancing blood circulation; Diminishing post-operative pain and swelling; Reducing wound healing time; treatment and assistance in healing of stasis dermatitis, venous stasis ulcers and… |
| Product code | JOW |
| Recalling firm | Medical Compression Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 11, 2012 |
| 510(k) numbers | K023573 |
| FEI number | 3003715046 |
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