Device recall
Z-3058-2011: Adjustable Vent Valve, TruChoice Alliant Healthcare Products REFERENCE#213-030…
FDA device recall · Class II · Alliant Enterprises LLC
Key facts
| Recall number (Z-number) | Z-3058-2011 |
|---|---|
| Recall event | 59524 |
| Product | Adjustable Vent Valve, TruChoice Alliant Healthcare Products REFERENCE#213-030 QUANTITY: 25 DESCRIPTION: ADJUSTABLE VENT VALVE, STERILE The TruChoice Vacuum Control One-Way Vent Valve is indicated for use during cardiopulmonary bypass surgery to help prevent the buildup of excess vacuum pressure… |
| Product code | MJJ |
| Recalling firm | Alliant Enterprises LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 23, 2012 |
| 510(k) numbers | K001245 |
| FEI number | 3004986960 |
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