Device recall
Z-0553-2009: Compression Sleeves Model #'s: HUNDVT10-1 and KEN5329 The SterilMed Intermittent…
FDA device recall · Class II · Sterilmed Inc
Key facts
| Recall number (Z-number) | Z-0553-2009 |
|---|---|
| Recall event | 49510 |
| Product | Compression Sleeves Model #'s: HUNDVT10-1 and KEN5329 The SterilMed Intermittent Compression Sleeve, 400 series used in conjunction with the Talley DVT-275 pump is indicated for any person that is at risk for deep vein thrombosis or could otherwise benefit from enhanced blood flow and circulation… |
| Product code | JOW |
| Recalling firm | Sterilmed Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 26, 2011 |
| 510(k) numbers | K003857 |
| FEI number | 3001237663 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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