Device recall
Z-3062-2011: TruChoice Alliant Healthcare Products, REFERENCE# SSD-100EX, QUANTITY: 25…
FDA device recall · Class II · Alliant Enterprises LLC
Key facts
| Recall number (Z-number) | Z-3062-2011 |
|---|---|
| Recall event | 59524 |
| Product | TruChoice Alliant Healthcare Products, REFERENCE# SSD-100EX, QUANTITY: 25, DESCRIPTION: TUBING W/ ONE WAY VALVE, STERILE The TrueChoice Vacuum Control One-Way Vent Valve is indicated for use during cardiopulmonary bypass surgery to help prevent the buildup of excess vacuum pressure when suctioning… |
| 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