Device recall
Z-0589-03: Scimed ChoICE PT ''J'' Tip 182 cm Guide Wire, a single use, sterile (EO), device…
FDA device recall · Class III · Symbiosis Corp.
Key facts
| Recall number (Z-number) | Z-0589-03 |
|---|---|
| Recall event | 25500 |
| Product | Scimed ChoICE PT ''J'' Tip 182 cm Guide Wire, a single use, sterile (EO), device packaged in a carrier tube, which is held in a coil by plastic clips. The carrier tube assembly of the guide wire is sealed into a pouch. The pouch assembies are packaged in a five-pack product box. |
| 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