Device recall
Z-0592-03: Product is a ChoICE 182 cm Guide Wire, intended to facilitate placement of…
FDA device recall · Class III · Symbiosis Corp.
Key facts
| Recall number (Z-number) | Z-0592-03 |
|---|---|
| Recall event | 25512 |
| Product | Product is a ChoICE 182 cm Guide Wire, intended to facilitate placement of balloon dilatation catheters and other therapeutic devices during Percutaneous Transluminal Coronary Angioplasty (PTCA) procedures. The ChoICE guide wire contains a one-piece stainless steel core, which extends throughout the… |
| Product code | DQX |
| Recalling firm | Symbiosis Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 15, 2008 |
| 510(k) numbers | K962572 |
| FEI number | 1051710 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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